WOUND DRESSING KIT— 510(k) K923905

Unknown

Kit Pak, Inc.

FDA 510(k) clearance K923905 for WOUND DRESSING KIT, Unknown on 1993-07-02. Applicant: Kit Pak, Inc.. Device class: 2.

Clearance details

Applicant: Kit Pak, Inc.
Product code: Code MCY
Device class: Class 2
Regulation: 21 CFR 880.5075
Advisory panel: General Hospital
Date received: 1992-08-04
Decision date: 1993-07-02
Decision: Unknown
Clearance type: Traditional
Location: Elk Grove Village, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MCY

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K960585 — WOUND CARE COMPRESSION SYSTEM (WCCS)1996-04-26
K952334 — DRESSING CHANGE TRAY1995-07-14
K951021 — CIRCULON SYSTEM STEP 21995-06-12

More clearances from Kit Pak, Inc.

K942959 — KIT PAK WET SALINE DRESSING1995-02-14
K941499 — KIT PAK DRESSING CHANGE TRAY1994-07-20
K932310 — KIT PAK INCONTINENT SKIN CARE KIT1994-06-01
K934080 — URINARY DRAINAGE BAG1994-05-18
K931013 — FOLEY CATHETER TRAY1993-08-09

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