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FDA 510(k)

AUTO FIRST-AID KIT FOR AMERICA

K-Number: K903393 · 1991-01-31

ApplicantHisler-Radke, Inc.
Decision Date1991-01-31
Product CodeLRR
DecisionUnknown

Device Summary

AUTO FIRST-AID KIT FOR AMERICA is the device name listed in this FDA 510(k) record. The listed applicant is Hisler-Radke, Inc.. It received FDA 510(k) clearance on 1991-01-31 under 510(k) number K903393. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the AUTO FIRST-AID KIT FOR AMERICA?

AUTO FIRST-AID KIT FOR AMERICA is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Hisler-Radke, Inc.. The 510(k) number is K903393.

When did AUTO FIRST-AID KIT FOR AMERICA receive FDA 510(k) clearance?

AUTO FIRST-AID KIT FOR AMERICA received FDA 510(k) clearance on 1991-01-31, under 510(k) number K903393.

Who is the listed applicant for AUTO FIRST-AID KIT FOR AMERICA?

The FDA 510(k) record lists Hisler-Radke, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO FIRST-AID KIT FOR AMERICA?

The FDA product code for AUTO FIRST-AID KIT FOR AMERICA is LRR.

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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.K940249CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSINGCertified Safety Mfg., Inc.K941311FIRST AID/TRUMA KITCertified Safety Mfg., Inc.K931058TICK-ATTACK(TM) KITMind Mechanics, Inc.K931634VARIOUS KITSPolymint Industrial Co. , Ltd.

Official Source

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

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