Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

GEI 1981-01-15

DUAL-TROL

Applicant Cimarron Instruments, Inc.

K-Number K802972

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NAB 1981-01-15

BONE-DRI SURGICAL SPONGE

Applicant Howmedica Corp.

K-Number K803125

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KDD 1981-01-15

SUTURE REMOVAL KIT

Applicant Walpak Co.

K-Number K803199

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KSB 1981-01-15

SUPER-SPIKE TRANSFER SET

Applicant Geneva Laboratories, Inc.

K-Number K802940

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GDB 1981-01-15

PENTAX UPPER G.I. FIBERSCOPE, #FG-34

Applicant Pentax Precision Instrument Corp.

K-Number K810007

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JJQ 1981-01-15

LKB-WALLACE 1250 LUMINOMETER

Applicant Lkb Instruments, Inc.

K-Number K803131

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CDP 1981-01-15

T3 RIABEAD DIAGNOSTIC KIT

Applicant Abbott Laboratories

K-Number K803261

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IYO 1981-01-15

MULTI-IMAGE CAMERA-#627 TLC

Applicant Dunn Systems, Inc.

K-Number K802905

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FMF 1981-01-15

IRRIGATION SET W/PISTON SYRINGE

Applicant Walpak Co.

K-Number K803198

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CAN 1981-01-15

REGULATOR, OXYGEN MECHANICAL

Applicant Timeter Instrument Corp.

K-Number K803207

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FYA 1981-01-15

L.A.F. ISOLATION PACK

Applicant Action Medical Systems, Inc.

K-Number K802885

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ILJ 1981-01-15

FOOT BATHS & HAND MASSAGERS

Applicant Associated Mills, Inc.

K-Number K810034

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