510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Circon Video

Santa Barbara, CA, US

Circon Video appears in FDA device records in Santa Barbara, CA. FDA records list 14 510(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
14
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 14 510(k) clearances for Circon Video between 1990 and 2002. The busiest year on record is 2001, with 7. The most recent is 2002, with 2.

Clearances by year, as a table
510(k) clearance decisions for Circon Video, by decision year
YearClearances
19901
19912
19931
19971
20017
20022
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K012758URETEROSCOPE, PEDIATRIC CYSTOURETEROSCOPE, OPERATING PEDIATRIC CYSTOURETEROSCOPE, MODELS MR-9, MR-9L,FGBSubstantially Equivalent
K011876DOLPHIN II FLUID MANAGEMENT SYSTEM, MODEL DOL-2HIGSubstantially Equivalent
K011849MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROSFGBSubstantially Equivalent
K012929FLEXIBLE PEDIATRIC CYSTOURETEROSCOPE, MODEL AUR- 735FAJSubstantially Equivalent
K012951APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPEFGBSubstantially Equivalent
K012925DUR-8, MODELS DUR-8FGBSubstantially Equivalent
K012265METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088FCWSubstantially Equivalent
K012153LOWSLEY SUPRAPUBIC TRACTORKOBSubstantially Equivalent
K011848CIRCON AEH-4 ELECTROHYDRAULIC LITHOTRIPSY PROBEFFKSubstantially Equivalent
K970595CIRCON ENDOTEK OM-4 H2O CYSTOMETRY PUMPFENSubstantially Equivalent
K914883CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURGGEISubstantially Equivalent
K914101CIRCON ACMI CAT.# LAP 9900; HIGH FLOW INSUFFLATORHIFSubstantially Equivalent
K911053CIRCON ACMI HYDROLAPAROSCOPE(TM) INSTRUMENTGCJSubstantially Equivalent
K890328ADULT RESECTOSCOPEHIHSubstantially 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