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FDA 510(k)

SHAWNEE PRODUCTS KIT II

K-Number: K921761 · 1993-03-18

ApplicantAbsentee Shawnee Bandage Group
Decision Date1993-03-18
Product CodeKGX
Advisory CommitteeHO
DecisionUnknown

Device Summary

SHAWNEE PRODUCTS KIT II 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 1993-03-18 under 510(k) number K921761. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SHAWNEE PRODUCTS KIT II?

SHAWNEE PRODUCTS KIT II is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Absentee Shawnee Bandage Group. The 510(k) number is K921761.

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

SHAWNEE PRODUCTS KIT II received FDA 510(k) clearance on 1993-03-18, under 510(k) number K921761.

Who is the listed applicant for SHAWNEE PRODUCTS KIT II?

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 II?

The FDA product code for SHAWNEE PRODUCTS KIT II is KGX.

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 IVK921762SHAWNEE PRODUCTS KIT I

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, Inc.

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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