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FDA 510(k)

WELMED, INC. SURGICAL GOWNS

K-Number: K070431 · 2007-05-24

ApplicantWelmed, Inc.
Decision Date2007-05-24
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WELMED, INC. SURGICAL GOWNS is the device name listed in this FDA 510(k) record. The listed applicant is Welmed, Inc.. It received FDA 510(k) clearance on 2007-05-24 under 510(k) number K070431. 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 WELMED, INC. SURGICAL GOWNS?

WELMED, INC. SURGICAL GOWNS is a medical device that received FDA 510(k) clearance on 2007-05-24. The listed applicant is Welmed, Inc.. The 510(k) number is K070431.

When did WELMED, INC. SURGICAL GOWNS receive FDA 510(k) clearance?

WELMED, INC. SURGICAL GOWNS received FDA 510(k) clearance on 2007-05-24, under 510(k) number K070431.

Who is the listed applicant for WELMED, INC. SURGICAL GOWNS?

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

What is the FDA product code for WELMED, INC. SURGICAL GOWNS?

The FDA product code for WELMED, INC. 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.

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Other records listing Welmed, 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.

K070432GENERAL SURGERY DRAPESK070936WELMED HYPODERMIC SYRINGE

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.

K260407Principle & Will ANSI/AAMI PB 70 (Sterile/Non-sterile) Level 3 Surgical Gowns (Reinforced) and Principle & Will ANSI/AMMI PB70 (Sterile/Non-sterile) Level 4 Surgical Gowns/Isolation GownsPrinciple & Will Co., Ltd.K261028Surgical Gown Level2 (S, M, L, XL, XXL, XXXL)Yadu Medical (Henan) Co., Ltd.K261949NYES Tuff Cuff L3 Disposable GownsNew York Embroidery StudioK252575Tuff Cuff™ Disposable Surgical Gowns AAMI L4 Sterile-Large (ML-L4-STL-DC-L)New York Embroidery Studio (NYES)K260725BAÜMER Surgical Gowns (COP01, COP04, COP05, COP10)Hindernis DE Mexico, S.A.P.I. DE C.V.K253243Cardinal Health™ Poly Reinforced Surgical GownCardinal Health 200, LLC

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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