Transidyne General Corp.
Transidyne General Corp. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1996.
Top product codes for Transidyne General Corp.
Recent clearances by Transidyne General Corp.
- K961217 — BODILY FLUID DISPOSAL KIT
- K955658 — LACERATION TRAY
- K950743 — ORAL PROCEDURE PACK
- K950773 — PROPHYLAXIS PACK
- K950449 — SURGICAL BUR
- K950403 — SURGICAL SAW BLADES
- K924811 — I.V. START KIT
- K924243 — TRACHEOSTOMY CARE KIT
- K922339 — SUTURE REMOVAL KIT
- K922041 — PRIMARY SURGICAL DRESSING TRAY
- K897133 — MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
- K896373 — 1400 SERIES EVIDENCE COLLECTION KIT
- K895202 — 1420 HEEL-STICK(TM) NEONATAL BLOOD SAMPLING KIT
- K891388 — 1570 - FETAL BLOOD SAMPLING KIT
- K831459 — FETAL BLOOD SAMPLING KIT #1560
- K812601 — SQC BUFFER
- K812552 — COROMETRICS MEDICAL SYST. 220 PH ANALY.
- K810028 — FETAL BLOOD SAMPLING KIT MODEL 1560
- K803240 — CORNING 760 FLUOROMETER/DENSITOMETER
- K800271 — COROMETRICS MEDICAL SYSTEMS 220 PH SYS.
- K780318 — MODULAR SCANNING DENSITOMETER SYS.
Data sourced from openFDA. This site is unofficial and independent of the FDA.