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FDA 510(k)

APPAREL, BARRIER SCRUB

K-Number: K760554 · 1976-11-12

Decision Date1976-11-12
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

APPAREL, BARRIER SCRUB is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760554. 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 APPAREL, BARRIER SCRUB?

APPAREL, BARRIER SCRUB is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Surgikos, Inc.. The 510(k) number is K760554.

When did APPAREL, BARRIER SCRUB receive FDA 510(k) clearance?

APPAREL, BARRIER SCRUB received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760554.

Who is the listed applicant for APPAREL, BARRIER SCRUB?

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

What is the FDA product code for APPAREL, BARRIER SCRUB?

The FDA product code for APPAREL, BARRIER SCRUB 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 Surgikos, 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 56 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

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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