Predissociation of Rydberg states of CO has been investigated by the C (³P and ¹D) and O (³P) photofragment measurements in the region of 103 000-114 000 cm^-1 (88-97 nm). The simulations of the rotational structures of np and nf Rydberg states were also carried out by using the l-uncoupling Hamiltonian model. The photofragment yield spectra were compared with the ion-dip spectra which correspond to the absorption spectra, indicating that all the Rydberg states, ns, np, nd, and nf converging to the X ²Σ⁺ CO⁺ ion, were subject to the predissociation. It was found that the lower member npπ and ndπ states exhibit two dissociation path ways, that is the C (³P) + O (³P) and the C (¹D) + O (³P) channels. Especially, for the 4pπ L ¹Π (v=0) state the two channels were found to be competitive with respect to parity as well as rotational quantum number J. At higher np series, such a parity and J-dependence of the predissociation disappeared, and the observed rotational structure was simulated very well by the model with no parity nor J dependence. For the ndσ states, the spectra of the 3dσ and 5dσ (v=0) states were diffuse, while the 4dσ (v=0) state showed a rotationally resolved photofragment yield spectrum. All the photofragment yield spectra of the nf (v=0) states exhibited sharp structures compared with those of other Rydberg states with a small l value. From a comparison between the photofragment yield spectrum and the ion-dip spectrum, it was found that the predissociation rate of the e-symmetry component is larger than that of the f-symmetry component. It was suggested that the e-symmetry levels predissociate through D&rquo; ¹Σ⁺ valence states, while the f-symmetry levels predissociate through the 2 ¹Π state.