Medical Device Manufacturer · US , Mchenry , IL

Transidyne General Corp. - FDA 510(k) Cleared Devices

21 submissions · 15 cleared · Since 1978

Total

Cleared

Denied

Transidyne General Corp. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1978 to 1996.

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

Transidyne General 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 - Transidyne General Corp.

21 devices

1-12 of 21

Cleared Jul 25, 1996

BODILY FLUID DISPOSAL KIT

K961217 · FXX

General Hospital · 119d

Cleared Jan 25, 1996

LACERATION TRAY

K955658 · FRG

General Hospital · 44d

General & Plastic Surgery · 26d

Cleared Feb 21, 1995

SURGICAL SAW BLADES

K950403 · GFA

General & Plastic Surgery · 21d

Cleared Jun 17, 1993

I.V. START KIT

K924811 · LRS

General & Plastic Surgery · 265d

Cleared Jun 16, 1993

TRACHEOSTOMY CARE KIT

K924243 · JOH

Anesthesiology · 296d

Cleared Dec 11, 1992

SUTURE REMOVAL KIT

K922339 · MCZ

General & Plastic Surgery · 206d

Cleared Nov 06, 1992

PRIMARY SURGICAL DRESSING TRAY

K922041 · FMF

General Hospital · 189d

Cleared Mar 30, 1990

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT

K897133 · CBT

Anesthesiology · 93d

Cleared Feb 26, 1990

1400 SERIES EVIDENCE COLLECTION KIT

K896373 · GIM

Pathology · 112d

Transidyne General Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Transidyne General Corp.

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