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FDA 510(k)

IMC SURGICAL GOWNS

K-Number: K052550 · 2005-11-17

Decision Date2005-11-17
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMC SURGICAL GOWNS is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medsurg Connection, Inc.. It received FDA 510(k) clearance on 2005-11-17 under 510(k) number K052550. 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 IMC SURGICAL GOWNS?

IMC SURGICAL GOWNS is a medical device that received FDA 510(k) clearance on 2005-11-17. The listed applicant is Intl. Medsurg Connection, Inc.. The 510(k) number is K052550.

When did IMC SURGICAL GOWNS receive FDA 510(k) clearance?

IMC SURGICAL GOWNS received FDA 510(k) clearance on 2005-11-17, under 510(k) number K052550.

Who is the listed applicant for IMC SURGICAL GOWNS?

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

What is the FDA product code for IMC SURGICAL GOWNS?

The FDA product code for IMC SURGICAL GOWNS 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 Intl. Medsurg Connection, 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.

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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