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FDA 510(k)

CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING

K-Number: K940249 · 1994-10-03

ApplicantCertified Safety Mfg., Inc.
Decision Date1994-10-03
Product CodeLRR
DecisionUnknown

Device Summary

CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Certified Safety Mfg., Inc.. It received FDA 510(k) clearance on 1994-10-03 under 510(k) number K940249. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING?

CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING is a medical device that received FDA 510(k) clearance on 1994-10-03. The listed applicant is Certified Safety Mfg., Inc.. The 510(k) number is K940249.

When did CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING receive FDA 510(k) clearance?

CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING received FDA 510(k) clearance on 1994-10-03, under 510(k) number K940249.

Who is the listed applicant for CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING?

The FDA 510(k) record lists Certified Safety Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING?

The FDA product code for CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING is LRR.

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Other records listing Certified Safety Mfg., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960587CPROTECTOR 2000K960615GAUZE COMPRESSK960624CERTI COOL INSTANT COLD COMPRESSK953102BLOODBORNE PATHOGEN KITK946338CERTIBURN BURN/TRAUMA FACE DRESSING, TOWEL DRESSINGK9450042, 3 & 4 BANDADGE COMPRESS

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Related Devices (Code: LRR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K964029EMERGENCY RELIEF KIT SYSTEMBaxter Healthcare CorpK952561WATER JEL BURN KITWater-Jel Technologies, Inc.K941311FIRST AID/TRUMA KITCertified Safety Mfg., Inc.K931058TICK-ATTACK(TM) KITMind Mechanics, Inc.K931634VARIOUS KITSPolymint Industrial Co. , Ltd.K921762SHAWNEE PRODUCTS KIT IAbsentee Shawnee Bandage Group

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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