J. Sklar Mfg. Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: JACOBS HIGH VACUUM SUCTION UNIT 05-2570, TISCHLER CERVICAL BIOPSY PUNCH FORCEPS, KOGAN ENDOSPECULUM 9-1/2
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - J. Sklar Mfg. Co., Inc. Ophthalmic ✕
3 devices