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

KNK 1982-12-20

URIC ACID REAGENT

Applicant Ac Biochemical Laboratories, Inc.

K-Number K822913

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N/A 1982-12-20

MAXICAMERA 500A SMALL FIELD IMAGING SYSTEM

Applicant General Electric Co.

K-Number K828545

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N/A 1982-12-20

MAXICAMERA 400ZS

Applicant General Electric Co.

K-Number K828544

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GTP 1982-12-19

STREPTACOCCUS CO-AGGLUTINATION KIT

Applicant American Scientific Products

K-Number K822799

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FRO 1982-12-17

CURITY TRANSPARENT FILM DRESSING

Applicant The Kendal Co.

K-Number K822424

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FOZ 1982-12-16

MULTI-LUMEN INTRAVENOUS CATHETER

Applicant Mcpherson Enterprises, Inc.

K-Number K823565

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BYX 1982-12-16

AUSTIN INHALATOR

Applicant Ems Industries, Inc.

K-Number K823246

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KDI 1982-12-16

AMICON DIAFILTERS 20 & 30 HEMOFILTERS

Applicant Amicon, Inc.

K-Number K823288

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JXG 1982-12-16

P-S MED. LUMBO PERITONEAL & VENTRICULO-

Applicant Pudenz-Schulte Medical Research Corp.

K-Number K823509

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KOC 1982-12-16

RENAFLO II

Applicant Renal Systems, Inc.

K-Number K823546

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HHD 1982-12-16

SURE & NATURAL MAXISHIELDS

Applicant Personal Products Co.

K-Number K823239

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FTT 1982-12-15

STEREOMED CAMERA

Applicant Diseases of the Skin Clinic, P.A.

K-Number K823534

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