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FDA 510(k)

EMERGENCY RELIEF KIT SYSTEM

K-Number: K964029 · 1997-03-17

ApplicantBaxter Healthcare Corp
Decision Date1997-03-17
Product CodeLRR
DecisionUnknown

Device Summary

EMERGENCY RELIEF KIT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1997-03-17 under 510(k) number K964029. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the EMERGENCY RELIEF KIT SYSTEM?

EMERGENCY RELIEF KIT SYSTEM is a medical device that received FDA 510(k) clearance on 1997-03-17. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K964029.

When did EMERGENCY RELIEF KIT SYSTEM receive FDA 510(k) clearance?

EMERGENCY RELIEF KIT SYSTEM received FDA 510(k) clearance on 1997-03-17, under 510(k) number K964029.

Who is the listed applicant for EMERGENCY RELIEF KIT SYSTEM?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY RELIEF KIT SYSTEM?

The FDA product code for EMERGENCY RELIEF KIT SYSTEM is LRR.

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Other records listing Baxter Healthcare Corp as applicant

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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.

K952561WATER 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.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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