PROMEDICAL SURGICAL GOWNS
K-Number: K042111 · 2004-12-10
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Device Summary
Frequently Asked Questions
What is the PROMEDICAL SURGICAL GOWNS?
PROMEDICAL SURGICAL GOWNS is a medical device that received FDA 510(k) clearance on 2004-12-10. The listed applicant is Promedical Products Co., Ltd.. The 510(k) number is K042111.
When did PROMEDICAL SURGICAL GOWNS receive FDA 510(k) clearance?
PROMEDICAL SURGICAL GOWNS received FDA 510(k) clearance on 2004-12-10, under 510(k) number K042111.
Who is the listed applicant for PROMEDICAL SURGICAL GOWNS?
The FDA 510(k) record lists Promedical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROMEDICAL SURGICAL GOWNS?
The FDA product code for PROMEDICAL 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 Promedical Products Co., Ltd. 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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