CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING— 510(k) K940249

Name: FDA 510(k) clearance K940249
Creator: U.S. Food and Drug Administration
Published: 1994-10-03

Unknown

Certified Safety Mfg., Inc.

FDA 510(k) clearance K940249 for CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING, Unknown on 1994-10-03. Applicant: Certified Safety Mfg., Inc.. Device class: Not classified.

Clearance details

Applicant: Certified Safety Mfg., Inc.
Product code: Code LRR
Device class: Not classified
Advisory panel: Unknown
Date received: 1994-01-19
Decision date: 1994-10-03
Decision: Unknown
Clearance type: Traditional
Location: Kansas City, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRR

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K964029 — EMERGENCY RELIEF KIT SYSTEM1997-03-17
K952561 — WATER JEL BURN KIT1995-07-14
K941311 — FIRST AID/TRUMA KIT1994-06-14
K931058 — TICK-ATTACK(TM) KIT1994-03-01
K931634 — VARIOUS KITS1993-11-30

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K960587 — CPROTECTOR 20001997-07-21
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K953102 — BLOODBORNE PATHOGEN KIT1995-12-11
K946338 — CERTIBURN BURN/TRAUMA FACE DRESSING, TOWEL DRESSING1995-03-29

Recalls naming K940249

K-number listed on FDA's recall record

Z-1060-2022 — The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2 tablets/packet, 25 packets/box; and Sinus Pain & Pressure, Product #81950, 2 tablets/packet, 25 packets/box. Product number and description: (1) K614-020 16PW - Firestone Supplemental - w/Logo; (2) KR614-020 16R - Firestone Supplemental - Refill; (3) K616-033 36M - Class A Office - Metal; (4) KR616-006 36R - Class A Office - Refill; (5) KR616-015 75R - Class A Office - Refill; (6) K616-015 75V - Class A Office - 3-Shelf Cabinet; (7) K618-016 EMT - Duke Energy TD - Red Bag; (8) KR618-016 EMTR - Duke Energy TD - Refill; (9) K616-008 FAC-3 - Class B + Meds - 3 Shelf Cabinet; (10) KR616-008 FAC-3R - Class B + Meds - Refill; (11) K618-013 FAC-3 - Five Star Safety - w/Logo; (12) K611-044 FAC-3 - Uline 100 person - w/Logo; (13) K620-609 FAC-3 - Uline Class B + Meds - w/Logo; (14) K616-072 FAC-4 - Choate Construction - w/Logo; (15) KR616-072 FAC-4R - Choate Construction - Refill; (16) K616-066 FAC-4 - Class B + Meds - 4 Shelf Cabinet; (17) KR616-066 FAC-4R - Class B + Meds - Refill; (18) K612-159 FAC-4 - Uline - w/Logo - w/Contents sticker; (19) K616-067 FAC-5 - Class B - 5 Shelf Cabinet; (20 KR616-067 FAC-5R - Class B - RefillClass II·Ongoing·Certified Safety Mfg Inc·20220405

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K940249.

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