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G.D. Searle and Co.

Mchenry, IL, US

G.D. Searle and Co. appears in FDA device records in Mchenry, IL. FDA records list 56 510(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
56
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

Showing 50 of 56

FDA records hold 56 510(k) clearances for G.D. Searle and Co. between 1976 and 1982. The busiest year on record is 1977, with 22. The most recent is 1982, with 1.

Clearances by year, as a table
510(k) clearance decisions for G.D. Searle and Co., by decision year
YearClearances
19765
197722
19784
19791
198015
19818
19821
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K821159IN-LINE OXYGEN MONITORING SYSTEMDRYSubstantially Equivalent
K811068BYPASS COILKPYSubstantially Equivalent
K811071VENOUS OXYGEN PROBECCESubstantially Equivalent
K803238INTRAVASCULAR CATHETERFOZSubstantially Equivalent
K810630SILICONE ELASTOMER COATED LATEX FOLEYKODSubstantially Equivalent
K810131ADMINISTRATION SETFPDSubstantially Equivalent
K802485SEARLE VASCULAR LOOPSKDCSubstantially Equivalent
K801805METRONIDAZOLE DISCSJWYSubstantially Equivalent
K810112SWR DISPOSABLE PREP RAZORKDCSubstantially Equivalent
K802280WHITE KNIGHT DRAPE SEALKKXSubstantially Equivalent
K802213WHITE KNIGHT BOVIE CORD/SUCTION TUBEKKXSubstantially Equivalent
K801415LATEX FOLEY CATHETER (HYDROMER COATED)KODSubstantially Equivalent
K801414ERYTHROCATH INTRAVENOUS CATHETER PLA. U.FOZSubstantially Equivalent
K800815ENTERAL & NASOGASTRIC SOL. ADMIN. SETKNTSubstantially Equivalent
K800929WHITE KNIGHT SURGICAL PACKFYASubstantially Equivalent
K800928WHITE KNIGHT SUPPLEMENTAL DRAPEKKXSubstantially Equivalent
K800927WHITE KNIGHT DISP. STERILE BACK GOWNFYASubstantially Equivalent
K800609CATHETER STYLETKODSubstantially Equivalent
K800611BOUGIE A BOULEKOESubstantially Equivalent
K800610URETHRAL SOUNDKOESubstantially Equivalent
K800608STONE DISLODGERFFLSubstantially Equivalent
K800607SUPRAPUBIC TROCARKOBSubstantially Equivalent
K800162ONCE TMHDWSubstantially Equivalent
K800139SEARLE PHO/SONIC ALPHA 2000IYOSubstantially Equivalent
K790285IMAGER, PHO/SONIC SERIES 2000IYOSubstantially Equivalent
K781508WATERPATH SCANNING OPTIONIYOSubstantially Equivalent
K781344OPTION PHO/SONIC B-MODE SCANNERIYOSubstantially Equivalent
K780855GAMMA CAMERAIYXSubstantially Equivalent
K772361LASER IMMUNONEPHELOMETRIC ANALYZERJQXSubstantially Equivalent
K771976ECG AMPLIFIER/R WAVE TRIGGERDRRSubstantially Equivalent
K772004HUMAN C4 COMPLEMENT CONTROL SERUMDBISubstantially Equivalent
K772003HUMAN REFERENCE SERUM C4 COMPLEMENTDAKSubstantially Equivalent
K772002PLATES FOR HUMAN C4 COMPLEMENTDBISubstantially Equivalent
K771934LINEAR ARRAY B-MODE SCANNERIYOSubstantially Equivalent
K771234TSH RIA REAGENT SETJLWSubstantially Equivalent
K771768GOAT LAMBDA-LIGHT CHAIN ANTI-HUMAN SERUMDEHSubstantially Equivalent
K771533DIGOXIN RIA KITDNJSubstantially Equivalent
K771180GAMMA GOUNTING SYS., AUTO, MODEL 1400JJJSubstantially Equivalent
K771239GOAT LAMBDA-LIGHT CHAIN ANTIHUMAN SERUMSubstantially Equivalent
K771238RID PLATES & INTENSI. FOR HUMAN IGE ETCDGCSubstantially Equivalent
K770773PIPETTE, DILUTING, MODEL ADP-30SDJQWSubstantially Equivalent
K770772PIPETTE, DISPENSING, MODEL ADP-30SDJQWSubstantially Equivalent
K770765REAGENT SET, RENORPACEDPASubstantially Equivalent
K770740RADIOASSAY TUBES & RADIOASSAY TUBE CAPSJJJSubstantially Equivalent
K770739SERUM SET, THYROID CONTROLCDPSubstantially Equivalent
K770738REAGENT, T-3 UPTAKECDPSubstantially Equivalent
K770737REAGENT SET, T-4, CPBCDXSubstantially Equivalent
K770677T-3 RIA REAGENT SETCDPSubstantially Equivalent
K770676T-4 RIA REAGENT SETCDXSubstantially Equivalent
K770220RADIONUCLIDE COMPUTED TOMOGRAPHY SYS.KPSSubstantially 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