J. Sklar Mfg. Co., Inc.
J. Sklar Mfg. Co., Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1984.
Top product codes for J. Sklar Mfg. Co., Inc.
Recent clearances by J. Sklar Mfg. Co., Inc.
- K843693 — JACOBS HIGH VACUUM SUCTION UNIT 05-2570
- K842112 — TISCHLER CERVICAL BIOPSY PUNCH FORCEPS
- K842111 — KOGAN ENDOSPECULUM 9-1/2
- K822448 — SCISSORS, VARIOUS
- K802457 — KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610
- K802458 — KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611
- K801273 — MAGILL CATHETER INTRO. FORCEPS
- K800441 — RUDD-CLINIC HEMORRHOIDAL FORCEPS
- K790577 — HEMORRHOIDAL LIGATOR
- K772229 — MINICLAMPS, STABILIZ., FALLOPIAN TUBE
- K772230 — CANNULA, PERFUSION, FALLOPIAN TUBE
- K771806 — THOREK SCISSORS 7 1/4 & 10
- K771344 — GUSBERG HYSTERECTOMY CLAMP
- K761334 — MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT
- K770040 — SCISSORS, STRABIMUS, 4 STRAIGHT
- K770041 — SCISSORS, STRABISMUS, 4 CURVED
- K761338 — LEFF STETHOSCOPE FOR FETAL HEART
- K770019 — SCISSORS, IRIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.