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FDA 510(k)

ORIGINAL TICK KIT/1ST AID KIT

K-Number: K895767 · 1989-12-22

ApplicantTick Kit, Inc.
Decision Date1989-12-22
Product CodeLRR
DecisionUnknown

Device Summary

ORIGINAL TICK KIT/1ST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Tick Kit, Inc.. It received FDA 510(k) clearance on 1989-12-22 under 510(k) number K895767. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the ORIGINAL TICK KIT/1ST AID KIT?

ORIGINAL TICK KIT/1ST AID KIT is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Tick Kit, Inc.. The 510(k) number is K895767.

When did ORIGINAL TICK KIT/1ST AID KIT receive FDA 510(k) clearance?

ORIGINAL TICK KIT/1ST AID KIT received FDA 510(k) clearance on 1989-12-22, under 510(k) number K895767.

Who is the listed applicant for ORIGINAL TICK KIT/1ST AID KIT?

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

What is the FDA product code for ORIGINAL TICK KIT/1ST AID KIT?

The FDA product code for ORIGINAL TICK KIT/1ST AID KIT 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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