Medical Device Manufacturer · US , Nevada City , CA

Healthtek, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Healthtek, Inc. has 9 FDA 510(k) cleared medical devices. Based in Nevada City, US.

Historical record: 9 cleared submissions from 1985 to 1993. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Healthtek, Inc. Filter by specialty or product code using the sidebar.

Healthtek, Inc. 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 - Healthtek, Inc.

9 devices

1-9 of 9

Cleared Jul 28, 1993

EMPTY SOLUTION TRANSFER CONTAINER W/ DETACH LEG

K923448 · KPE

General Hospital · 379d

Cleared Mar 18, 1992

TRANSFER-AID(TM)

K913985 · LHI

General Hospital · 195d

Cleared Nov 29, 1991

SNAPPER

K913608 · KPE

General Hospital · 107d

Cleared May 23, 1988

ADFUSE(TM)

K881590 · FRN

General Hospital · 40d

Cleared Feb 16, 1988

ADCOMP 4000 HP SYSTEM

K874495 · LHI

General Hospital · 106d

Cleared Oct 23, 1987

RETROBULBAR NEEDLE

K873848 · GDM

General & Plastic Surgery · 31d

Cleared Jul 08, 1986

ADCOMP

K860610 · LHI

General Hospital · 139d

Cleared May 30, 1986

FAST FLOW XX (AQUEOUS SOLUTION FILTER)

K860372 · FPB

General Hospital · 116d

Cleared Nov 13, 1985

STATLOCK

K854008 · LHI

General Hospital · 44d

Healthtek, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Healthtek, Inc.

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