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FDA 510(k)

KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE

K-Number: K871501 · 1987-06-02

ApplicantFraass Survival Systems, Inc.
Decision Date1987-06-02
Product CodeLRR
DecisionSubstantially Equivalent

Device Summary

KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE is the device name listed in this FDA 510(k) record. The listed applicant is Fraass Survival Systems, Inc.. It received FDA 510(k) clearance on 1987-06-02 under 510(k) number K871501. The device is classified under product code LRR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE?

KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE is a medical device that received FDA 510(k) clearance on 1987-06-02. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K871501.

When did KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE receive FDA 510(k) clearance?

KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE received FDA 510(k) clearance on 1987-06-02, under 510(k) number K871501.

Who is the listed applicant for KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE?

The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE?

The FDA product code for KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE is LRR.

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Other records listing Fraass Survival Systems, 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.

K912022FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZESK871458SURVIVAL KIT, INDIVIDUAL, TROP, TACTICAL AIR CREWK871434MEDICAL PACKET, INDIVIDUAL SURVIVAL KIT, AIRMAN'SK871437SURVIVAL KIT, INDIVIDUALK871916FRASTEC DRY BURN DRESSINGK871917FRASTEC DRY GAUZE BANDAGE

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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

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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