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.

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

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