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

DTB 1979-06-11

MODEL 6971 W/ DBS WIRE

Applicant Medtronic Vascular

K-Number K790988

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KFZ 1979-06-11

ULTRASONIC HUMIDIFIER

Applicant Hankscraft Div. of Gerber Products Co.

K-Number K790966

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DWF 1979-06-11

AORTIC ROOT CANNULA

Applicant Dlp, Inc.

K-Number K790565

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FOZ 1979-06-11

CATHETER METAL HUB/NONRADIOPAQUE

Applicant Jelco Laboratories

K-Number K790968

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DPS 1979-06-11

MODEL 78501A PATIENT MONITORING SYSTEM

Applicant Hewlett-Packard Co.

K-Number K790939

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DTR 1979-06-11

HEAT EXCHANGER COIL

Applicant Delta Medical Industries

K-Number K790756

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FCE 1979-06-07

CLAYTON COLON CLEANSING KIT

Applicant Clayton Medical Products, Inc.

K-Number K790535

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DIT 1979-06-06

DRUG ABUSE DIPSTICKS

Applicant Technical Resources, Inc.

K-Number K790805

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DRT 1979-06-06

STRESS TESTING SYSTEM, LATERAL TILTING

Applicant Engineering Dynamics Corp.

K-Number K790545

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GYB 1979-06-05

MEDI-TRACE EEG CREME

Applicant Graphic Controls Corp.

K-Number K790818

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KKX 1979-06-05

KIMLON IMPERVIOUS STOCKINETTES

Applicant Kimberly-Clark Corp.

K-Number K790972

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GEN 1979-06-05

FORCEPS #101 AND #102

Applicant C. Intl.

K-Number K790854

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