Medical Device Manufacturer · US , Austin , TX

Metatech Corp. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1985

13

Total

13

Cleared

0

Denied

Metatech Corp. has 13 FDA 510(k) cleared medical devices. Based in Austin, US.

Historical record: 13 cleared submissions from 1985 to 1993.

Browse the FDA 510(k) cleared devices submitted by Metatech Corp. Filter by specialty or product code using the sidebar.

Metatech Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Metatech Corp.

13 devices

1-13 of 13

Cleared Feb 12, 1993

MOBILE STANDING FRAME

Physical Medicine · 170d

Cleared Feb 07, 1992

COPPER VAPOR LASER SYSTEM

General & Plastic Surgery · 72d

Cleared Sep 19, 1990

VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LES

General & Plastic Surgery · 28d

Cleared Mar 24, 1989

HEXASCAN SCANNER HANDPIECE

General & Plastic Surgery · 31d

Cleared Nov 04, 1988

METALASER VASCULASE

General & Plastic Surgery · 77d

Cleared Oct 27, 1988

MODIFIED MODEL 2001 FIBER OPTICS CATHETER

Neurology · 90d

Cleared Sep 22, 1988

EVENT MARKER & A SECOND PRESSURE TREND OUTPUT

Neurology · 37d

Cleared Sep 08, 1988

METATECH ROBINSON BOLT ACCESSORY

Neurology · 79d

Cleared Aug 25, 1988

METATECH MICROCLIP APPLICATOR

Cardiovascular · 78d

Cleared Jul 18, 1988

EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET

Neurology · 47d

Cleared Jun 22, 1988

METATECH METAL MICROCLIP

Cardiovascular · 77d

Cleared Mar 28, 1988

METATECH INTRACRANIAL PRESSURE MONITORING SYSTEM

Neurology · 75d

Cleared Apr 03, 1985

BED SENTRY, MODEL 50U

Gastroenterology & Urology · 51d