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FDA 510(k)

GLENROE PLASTIC BRACKET

K-Number: K932920 · 1993-08-24

Decision Date1993-08-24
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GLENROE PLASTIC BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Glenroe Technologies. It received FDA 510(k) clearance on 1993-08-24 under 510(k) number K932920. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLENROE PLASTIC BRACKET?

GLENROE PLASTIC BRACKET is a medical device that received FDA 510(k) clearance on 1993-08-24. The listed applicant is Glenroe Technologies. The 510(k) number is K932920.

When did GLENROE PLASTIC BRACKET receive FDA 510(k) clearance?

GLENROE PLASTIC BRACKET received FDA 510(k) clearance on 1993-08-24, under 510(k) number K932920.

Who is the listed applicant for GLENROE PLASTIC BRACKET?

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

What is the FDA product code for GLENROE PLASTIC BRACKET?

The FDA product code for GLENROE PLASTIC BRACKET is DYW.

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.

Other records listing Glenroe Technologies 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.

View all 8 devices →

Related Devices (Code: DYW)

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.

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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