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

KGZ 1981-03-24

PERI-PATCH PERITONEAL CATHETER EXTENSION

Applicant Quinton, Inc.

K-Number K810531

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EMA 1981-03-24

PCA PERIOCARE PERIODONTAL DRESSING

Applicant Pulpdent Corp. of America

K-Number K810545

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N/A 1981-03-24

HOFFMAN HOOP DEVICE

Applicant Howmedica Corp.

K-Number K810644

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DYH 1981-03-24

INSTA-BOND

Applicant Lee Pharmaceuticals

K-Number K810517

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JIS 1981-03-24

EMIT-TFG PRISMA THYROXINE CALIBRATORS

Applicant Syva Co.

K-Number K810587

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KDJ 1981-03-24

CCPD CYCLER SET

Applicant American Medical Products, Inc.

K-Number K810670

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EBF 1981-03-24

SILUX RESTORATIVE MATERIAL & ENAMEL BOND

Applicant 3M Company

K-Number K810595

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EJH 1981-03-24

FULCAST/SUMMIT CASTING ALLOY

Applicant C.Vaupel Dental, Inc.

K-Number K810611

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EJH 1981-03-24

CRYSTALLOY-P

Applicant Shofu Dental Corp.

K-Number K810594

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KIT 1981-03-23

FUNGIZONE

Applicant Dutchland Laboratories, Inc.

K-Number K810784

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HRY 1981-03-20

MILLER MULTI-RADIUS TOTAL KNEE

Applicant Zimmer, Inc.

K-Number K810616

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GAA 1981-03-20

MSI BONE MARROW BIOPSY NEEDLE W/J TIP

Applicant Creative Research and Mfg., Inc.

K-Number K810248

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