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FDA 510(k)

MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN)

K-Number: K850177 · 1985-02-21

Decision Date1985-02-21
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Medica, Inc.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850177. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN)?

MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K850177.

When did MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) receive FDA 510(k) clearance?

MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850177.

Who is the listed applicant for MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN)?

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

What is the FDA product code for MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN)?

The FDA product code for MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN) is FYA.

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 Matrix Medica, Inc. 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 14 devices →

Related Devices (Code: FYA)

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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