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

Mchenry, IL, US

Microvasive 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 Microvasive between 1983 and 1987. The busiest year on record is 1985, with 5. The most recent is 1987, with 2.

Clearances by year, as a table
510(k) clearance decisions for Microvasive, by decision year
YearClearances
19833
19844
19855
19864
19872
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K872771LOW PROFILE GASTROSTOMYKNTSubstantially Equivalent
K870705THERMAL COAGULATORKNSSubstantially Equivalent
K861323REPLACEMENT GASTROSTOMY TUBEKNTSubstantially Equivalent
K861309JEJUNAL FEEDING TUBEKNTSubstantially Equivalent
K860589INFLATOR/DEFLATOR PISTON SYRINGEKNTSubstantially Equivalent
K860366CHALLENGER HOT BIOPSY FORCEPSKNSSubstantially Equivalent
K854238NEEDLE W/STYLET FOR IMPLANTATIONGAASubstantially Equivalent
K854063MICROVASIVE SILICONE SPRAYKCTSubstantially Equivalent
K851652PAPILLOTOMEKNSSubstantially Equivalent
K850393FLEXIBLE FIBEROPTIC ENDOSCOPESubstantially Equivalent
K844769RIGID FIBEROPITC ENDOSCOPEGCMSubstantially Equivalent
K841330GASTROSTOMY FEEDING TUBEKNTSubstantially Equivalent
K834468DRAINAGE STENTFGESubstantially Equivalent
K840033HYPODERMIC NEEDLES & STYLETSFMISubstantially Equivalent
K834467SPECIMEN TRAPBYZSubstantially Equivalent
K833417ENDOSCOPIC RETROGRADEODDSubstantially Equivalent
K833331ASPIRATION & IRRIGATION CATHETEROCXSubstantially Equivalent
K833330MUTO BRUSHFDXSubstantially 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