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

FMF 1978-12-12

PUNCTURE KIT, DISPOSALBE VEIN

Applicant Arrow Intl., Inc.

K-Number K781978

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KGZ 1978-12-12

ADAPTER, CATHETER SHEATH

Applicant Arrow Intl., Inc.

K-Number K781846

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FPA 1978-12-12

MODEL IV 1500 STANDARD BURETTE

Applicant Valleylab, Inc.

K-Number K781637

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GCX 1978-12-12

SUCTION APPARATUS, POWERED BY COMP. AIR

Applicant Farley, W.T.

K-Number K781988

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FSY 1978-12-12

9100 DAYSTAR AND 9110 ORBITER PACKAGE

Applicant Castle Co.

K-Number K781887

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CBK 1978-12-12

VENTILATOR, PRESSURE

Applicant Thompson Respiration Products, Inc.

K-Number K781159

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BTR 1978-12-12

ADAPTER, C/D SUCTION

Applicant Novametrix Medical Systems, Inc.

K-Number K781713

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LDD 1978-12-12

DEFIBRILLATOR, MARK II

Applicant Ipco Corp.

K-Number K781678

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DTE 1978-12-11

PULSE GENERATOR, MODEL 240, EXTERNAL

Applicant Intermedics, Inc.

K-Number K781327

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CBK 1978-12-11

RESPIRATOR, BANTAM MODEL

Applicant Thompson Respiration Products, Inc.

K-Number K781161

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CBT 1978-12-11

TRAY, ARTERIAL BLOOD GAS SAMPLING

Applicant Jelco Laboratories

K-Number K781857

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DTB 1978-12-08

PACING LEAD MODEL MVM 860, MVM 890

Applicant R.E. Brown Co., Inc.

K-Number K781625

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