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FDA 510(k)

CARLO SURGICAL GOWN

K-Number: K051426 · 2005-08-02

Decision Date2005-08-02
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARLO SURGICAL GOWN is the device name listed in this FDA 510(k) record. The listed applicant is Sofilm Technology Co., Ltd.. It received FDA 510(k) clearance on 2005-08-02 under 510(k) number K051426. 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 CARLO SURGICAL GOWN?

CARLO SURGICAL GOWN is a medical device that received FDA 510(k) clearance on 2005-08-02. The listed applicant is Sofilm Technology Co., Ltd.. The 510(k) number is K051426.

When did CARLO SURGICAL GOWN receive FDA 510(k) clearance?

CARLO SURGICAL GOWN received FDA 510(k) clearance on 2005-08-02, under 510(k) number K051426.

Who is the listed applicant for CARLO SURGICAL GOWN?

The FDA 510(k) record lists Sofilm Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARLO SURGICAL GOWN?

The FDA product code for CARLO 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.

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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