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FDA 510(k)

INGROWN TOENAIL PAD

K-Number: K923662 · 1993-04-20

ApplicantMany Bee Co.
Decision Date1993-04-20
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INGROWN TOENAIL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Many Bee Co.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K923662. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INGROWN TOENAIL PAD?

INGROWN TOENAIL PAD is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Many Bee Co.. The 510(k) number is K923662.

When did INGROWN TOENAIL PAD receive FDA 510(k) clearance?

INGROWN TOENAIL PAD received FDA 510(k) clearance on 1993-04-20, under 510(k) number K923662.

Who is the listed applicant for INGROWN TOENAIL PAD?

The FDA 510(k) record lists Many Bee Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INGROWN TOENAIL PAD?

The FDA product code for INGROWN TOENAIL PAD is KGX.

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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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