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Intramed Laboratories, Inc.

San Diego, CA, US

Intramed Laboratories, Inc. appears in FDA device records in San Diego, 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 Intramed Laboratories, Inc. between 1987 and 1996. The busiest year on record is 1990, with 5. The most recent is 1996, with 1.

Clearances by year, as a table
510(k) clearance decisions for Intramed Laboratories, Inc., by decision year
YearClearances
19871
19881
19905
19922
19943
19951
19961
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K953258TITANIUM HEMOSTATIC CLIPFZPSubstantially Equivalent
K942457GRAFT THROMBECTOMY INSTRUMENTSMCWSubstantially Equivalent
K931792ARTHROSCOPEHRHSubstantially Equivalent
K925283VALVULOTOMEMGZSubstantially Equivalent
K934696ANGIOSCOPELYKSubstantially Equivalent
K922114ENDOSCOPIC RETRIEVAL BASKETFFLSubstantially Equivalent
K914385OPTICAL VALVULOTOMEMGZSubstantially Equivalent
K904465FLEXIBLE ARTHROSCOPEHRXSubstantially Equivalent
K903528LAPAROSCOPEHETSubstantially Equivalent
K902444CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMPDQISubstantially Equivalent
K901010FLEXIBLE CHOLEDOCHOSCOPEFBNSubstantially Equivalent
K894459ANGIOSCOPELYKSubstantially Equivalent
K882761TRANSERVICAL ENDOSCOPE (HYSTEROSCOPE)HIHSubstantially Equivalent
K872282FLEXIBLE URETEROSCOPEFGBSubstantially 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