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

BTT 1982-03-12

EAST AUTOCLAVE HUMIDIFIER

Applicant Cairco , Ltd.

K-Number K812957

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DRS 1982-03-12

MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS

Applicant Graphic Controls Corp.

K-Number K820457

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DTL 1982-03-12

WM. HARVEY OVERPRESSURE SAFETY VALVE

Applicant C.R. Bard, Inc.

K-Number K820297

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KXZ 1982-03-12

THERMASCAN

Applicant Bcd Products, Inc.

K-Number K813547

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CBK 1982-03-12

ANESTHESIA VENTILATOR

Applicant Puritan Bennett Corp.

K-Number K820393

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DXN 1982-03-12

PATIENT FOLLOW-UP COMPUTER (PFC

Applicant Medical Systems, Inc.

K-Number K820402

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FMF 1982-03-12

PHARMACEUTICALS MOD. 1CC-1,2,3 THRU 50CC

Applicant Abek Corp.

K-Number K820449

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NAB 1982-03-12

AEGIS NON-ADHERENT DRESSING

Applicant Professional Medical Products, Inc.

K-Number K820413

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KHX 1982-03-12

HEART-ALERT

Applicant Medical Equipment Devices, Inc.

K-Number K820444

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GCX 1982-03-12

IMPACT, MODEL 310

Applicant Impact Instrumentation, Inc.

K-Number K820424

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NHK 1982-03-12

DISP. HYPERINFLATION BAG SYSTEM

Applicant Intec Medical, Inc.

K-Number K813317

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CAP 1982-03-12

MONITRON MODEL JL-7

Applicant Florida Medical Equipment Repair, Inc.

K-Number K820353

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