Spontaneous resting-state neural activity or hemodynamics has been used to reveal functional connectivity in the brain. However, most of the commonly used clustering algorithms for functional parcellation are time-consuming, especially for high-resolution imaging data. We propose a density center-based fast clustering (DCBFC) method that can rapidly perform the functional parcellation of isocortex. DCBFC was validated using both simulation data and the spontaneous calcium signals from widefield fluorescence imaging of excitatory neuron-expressing transgenic mice (Vglut2-GCaMP6s). Compared to commonly used clustering methods such as k-means, hierarchical, and spectral, DCBFC showed a higher adjusted Rand index when the signal-to-noise ratio was greater than −8  dB for simulated data and higher silhouette coefficient for in vivo mouse data. The resting-state functional connectivity (RSFC) patterns obtained by DCBFC were compared with the anatomic axonal projection density (PDs) maps derived from the voxel-scale model. The results showed a high spatial correlation between RSFC patterns and PDs.