SUTURE REMOVAL KIT— 510(k) K922339

Unknown

Transidyne General Corp.

FDA 510(k) clearance K922339 for SUTURE REMOVAL KIT, Unknown on 1992-12-11. Applicant: Transidyne General Corp.. Device class: 1.

Clearance details

Applicant: Transidyne General Corp.
Product code: Code MCZ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-05-19
Decision date: 1992-12-11
Decision: Unknown
Clearance type: Traditional
Location: Spartanburg, SC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MCZ

K050656 — AMSINO SUTURE REMOVAL KIT2005-05-02
K964827 — PROD. NO. 01-132 - SUTURE REMOVAL KIT1997-02-14
K963714 — GRAND MEDICAL SUTURE REMOVAL KIT1996-11-27
K943046 — SKIN STAPLE REMOVAL TRAYS1994-07-29
K941465 — SUTURE REMOVAL KIT1994-04-22

More clearances from Transidyne General Corp.

K961217 — BODILY FLUID DISPOSAL KIT1996-07-25
K955658 — LACERATION TRAY1996-01-25
K950743 — ORAL PROCEDURE PACK1995-03-31
K950773 — PROPHYLAXIS PACK1995-03-31
K950449 — SURGICAL BUR1995-03-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.