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FDA 510(k)

PETIT BANDS

K-Number: K843587 · 1984-11-27

ApplicantMicori Gifts, Inc.
Decision Date1984-11-27
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PETIT BANDS is the device name listed in this FDA 510(k) record. The listed applicant is Micori Gifts, Inc.. It received FDA 510(k) clearance on 1984-11-27 under 510(k) number K843587. 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 PETIT BANDS?

PETIT BANDS is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Micori Gifts, Inc.. The 510(k) number is K843587.

When did PETIT BANDS receive FDA 510(k) clearance?

PETIT BANDS received FDA 510(k) clearance on 1984-11-27, under 510(k) number K843587.

Who is the listed applicant for PETIT BANDS?

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

What is the FDA product code for PETIT BANDS?

The FDA product code for PETIT BANDS 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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