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

BXX 1978-07-17

PERCI

Applicant Micro Tronics Corp.

K-Number K780838

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GAD 1978-07-17

AUTOMATIC RETRACTOR HOLDER

Applicant Great Eastern Lumber Co., Inc.

K-Number K780708

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HWT 1978-07-17

KNEE INSTRUMENTATION, CONDYLAR

Applicant Biomet, Inc.

K-Number K781091

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HIN 1978-07-17

ONE INCISION BI-POLAR ELECTRO. FORCEPS

Applicant Kli

K-Number K781089

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CBA 1978-07-17

CUFF PACER

Applicant Omp Laboratories, Inc.

K-Number K780703

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N/A 1978-07-17

CAST WEDGE, YANCEY

Applicant Orthopedic Equipment Co., Inc.

K-Number K781112

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FJG 1978-07-17

LUNDIA PLATE DISPOSABLE DIALYZER

Applicant Gambro, Inc.

K-Number K780700

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KOB 1978-07-17

PERCUTANEOUS SURAPUBIC CATHETER

Applicant Vance Products, Inc.

K-Number K780765

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ESD 1978-07-17

HEARING AID, EYEGLASS, B-12

Applicant Argosy Intl. (Usa), Inc.

K-Number K781096

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ESD 1978-07-17

HEARING AID, EYEGLASS

Applicant Argosy Intl. (Usa), Inc.

K-Number K781094

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FZT 1978-07-17

SUTURE CUTTER

Applicant Laschal Instrument Corp.

K-Number K780574

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IXQ 1978-07-17

PLURIX C; RADIOGRAPHIC TABLE

Applicant Tecnomed, Inc.

K-Number K781066

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