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FDA 510(k)

TICK-ATTACK(TM) KIT

K-Number: K931058 · 1994-03-01

ApplicantMind Mechanics, Inc.
Decision Date1994-03-01
Product CodeLRR
DecisionUnknown

Device Summary

TICK-ATTACK(TM) KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mind Mechanics, Inc.. It received FDA 510(k) clearance on 1994-03-01 under 510(k) number K931058. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the TICK-ATTACK(TM) KIT?

TICK-ATTACK(TM) KIT is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Mind Mechanics, Inc.. The 510(k) number is K931058.

When did TICK-ATTACK(TM) KIT receive FDA 510(k) clearance?

TICK-ATTACK(TM) KIT received FDA 510(k) clearance on 1994-03-01, under 510(k) number K931058.

Who is the listed applicant for TICK-ATTACK(TM) KIT?

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

What is the FDA product code for TICK-ATTACK(TM) KIT?

The FDA product code for TICK-ATTACK(TM) 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.K931634VARIOUS KITSPolymint Industrial Co. , Ltd.K921762SHAWNEE PRODUCTS KIT IAbsentee Shawnee Bandage Group

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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