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

FMQ 1977-09-30

BODY RESTRAINT

Applicant Medical Restraints, Inc.

K-Number K771636

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FCW 1977-09-30

PENTAX LH-150F LIGHT SOURCE

Applicant Pilling Co.

K-Number K771739

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FMQ 1977-09-30

PATIENT RESTRAINT SYSTEM

Applicant Mtd, Inc.

K-Number K771659

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FMQ 1977-09-30

LIMB RESTRAINT

Applicant Medical Restraints, Inc.

K-Number K771630

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GAG 1977-09-30

AUTO SUTURE R CLIP INSTRUMENT

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K771113

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GDO 1977-09-30

SUTURE CLIP REMOVER

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K771640

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DXS 1977-09-30

CORONARY PRESSURE PERFUSION PUMP

Applicant 3M Health Care, Sarns

K-Number K771764

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EXB 1977-09-30

COLORPLAST TRANSVERSE SYSTEM

Applicant C.R. Bard, Inc.

K-Number K771775

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BXN 1977-09-30

MYO-CHECK

Applicant Med General

K-Number K771765

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FZP 1977-09-30

AUTO SUTURE R CLIP

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K771112

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GEI 1977-09-30

ELECTROSURGICAL POWER GENERATORS

Applicant Aspen Laboratories, Inc.

K-Number K771007

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FMQ 1977-09-30

HAND RESTRAINT

Applicant Medical Restraints, Inc.

K-Number K771629

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