510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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J. Sklar Mfg. Co., Inc.

Mchenry, IL, US

J. Sklar Mfg. Co., Inc. appears in FDA device records in Mchenry, IL. FDA records list 18 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
18
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 18 510(k) clearances for J. Sklar Mfg. Co., Inc. between 1977 and 1984. The busiest year on record is 1977, with 7. The most recent is 1984, with 3.

Clearances by year, as a table
510(k) clearance decisions for J. Sklar Mfg. Co., Inc., by decision year
YearClearances
19777
19782
19791
19802
19812
19821
19843
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K843693JACOBS HIGH VACUUM SUCTION UNIT 05-2570BTASubstantially Equivalent
K842112TISCHLER CERVICAL BIOPSY PUNCH FORCEPSHFBSubstantially Equivalent
K842111KOGAN ENDOSPECULUM 9-1/2HTZSubstantially Equivalent
K822448SCISSORS, VARIOUSFZTSubstantially Equivalent
K802458KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611HFBSubstantially Equivalent
K802457KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610HFBSubstantially Equivalent
K801273MAGILL CATHETER INTRO. FORCEPSKOASubstantially Equivalent
K800441RUDD-CLINIC HEMORRHOIDAL FORCEPSKOASubstantially Equivalent
K790577HEMORRHOIDAL LIGATORHCFSubstantially Equivalent
K772230CANNULA, PERFUSION, FALLOPIAN TUBELKFSubstantially Equivalent
K772229MINICLAMPS, STABILIZ., FALLOPIAN TUBEHCZSubstantially Equivalent
K771806THOREK SCISSORS 7 1/4 & 10FZTSubstantially Equivalent
K771344GUSBERG HYSTERECTOMY CLAMPHGCSubstantially Equivalent
K761334MARCUSE TUBE CLAMPING FORCEPS, STRAIGHTGENSubstantially Equivalent
K770041SCISSORS, STRABISMUS, 4 CURVEDHNFSubstantially Equivalent
K770040SCISSORS, STRABIMUS, 4 STRAIGHTHNFSubstantially Equivalent
K770019SCISSORS, IRISHNFSubstantially Equivalent
K761338LEFF STETHOSCOPE FOR FETAL HEARTHGNSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain