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FDA 510(k)

STUART LEE CLIP

K-Number: K881741 · 1988-06-03

ApplicantStuart-Lee, Inc.
Decision Date1988-06-03
Product CodeGDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STUART LEE CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Stuart-Lee, Inc.. It received FDA 510(k) clearance on 1988-06-03 under 510(k) number K881741. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STUART LEE CLIP?

STUART LEE CLIP is a medical device that received FDA 510(k) clearance on 1988-06-03. The listed applicant is Stuart-Lee, Inc.. The 510(k) number is K881741.

When did STUART LEE CLIP receive FDA 510(k) clearance?

STUART LEE CLIP received FDA 510(k) clearance on 1988-06-03, under 510(k) number K881741.

Who is the listed applicant for STUART LEE CLIP?

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

What is the FDA product code for STUART LEE CLIP?

The FDA product code for STUART LEE CLIP is GDJ.

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Related Devices (Code: GDJ)

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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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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