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

FYA 1976-08-11

GOWN, BOUNDARY SINGLE USE REINFORCED

Applicant Procter & Gamble Mfg. Co.

K-Number K760237

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FOZ 1976-08-11

KIT, CATHETER

Applicant Jelco Laboratories

K-Number K760319

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FPY 1976-08-11

BLANKET, BURN

Applicant Winn Hirsch & Assoc.

K-Number K760365

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BZQ 1976-08-11

RESPIRATORY SUPPORT SYSTEM, NEONATAL

Applicant Sherwood Medical Industries

K-Number K760340

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DCK 1976-08-11

TEST, SLIDE FOR C-REATIVE PROTEIN

Applicant Icl Scientific

K-Number K760354

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CAZ 1976-08-11

TRAY, CURITY CONTINUOUS EPIDURAL

Applicant Kendall Research Center

K-Number K760343

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FSE 1976-08-11

I.V. SUPPORT, TECNOL ARMBOARD

Applicant Tecnol New Jersey Wound Care, Inc.

K-Number K760308

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CGR 1976-08-11

TEST SYSTEM, RIA CORTISOL

Applicant Corning Medical & Scientific

K-Number K760256

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LDQ 1976-08-11

RAZOR, SCHICK DISPOSABLE

Applicant Parke-Davis Co.

K-Number K760342

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EYQ 1976-08-11

UNDERPAD CODE NO. 8453

Applicant Johnson & Johnson Professionals, Inc.

K-Number K760277

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CAZ 1976-08-11

CIRCUIT, INTENSIVE CARE VENTILATOR

Applicant Monaghan Medical Corp.

K-Number K760352

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N/A 1976-08-11

PROBECOT II

Applicant Measurement-Science Corp.

K-Number K760242

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