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FDA 510(k)

SHAWNEE PRODUCTS KIT I

K-Number: K921762 · 1993-01-06

ApplicantAbsentee Shawnee Bandage Group
Decision Date1993-01-06
Product CodeLRR
DecisionUnknown

Device Summary

SHAWNEE PRODUCTS KIT I is the device name listed in this FDA 510(k) record. The listed applicant is Absentee Shawnee Bandage Group. It received FDA 510(k) clearance on 1993-01-06 under 510(k) number K921762. The device is classified under product code LRR. FDA Decision: Unknown.

Frequently Asked Questions

What is the SHAWNEE PRODUCTS KIT I?

SHAWNEE PRODUCTS KIT I is a medical device that received FDA 510(k) clearance on 1993-01-06. The listed applicant is Absentee Shawnee Bandage Group. The 510(k) number is K921762.

When did SHAWNEE PRODUCTS KIT I receive FDA 510(k) clearance?

SHAWNEE PRODUCTS KIT I received FDA 510(k) clearance on 1993-01-06, under 510(k) number K921762.

Who is the listed applicant for SHAWNEE PRODUCTS KIT I?

The FDA 510(k) record lists Absentee Shawnee Bandage Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHAWNEE PRODUCTS KIT I?

The FDA product code for SHAWNEE PRODUCTS KIT I is LRR.

Related Clinical Trials

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.

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Other records listing Absentee Shawnee Bandage Group 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.

K923319SHAWNEE PRODUCT KIT IVK921761SHAWNEE PRODUCTS KIT II

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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