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FDA 510(k)

PROMEDICAL SURGICAL DRAPES

K-Number: K042131 · 2004-12-10

Decision Date2004-12-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROMEDICAL SURGICAL DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is Promedical Products Co., Ltd.. It received FDA 510(k) clearance on 2004-12-10 under 510(k) number K042131. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROMEDICAL SURGICAL DRAPES?

PROMEDICAL SURGICAL DRAPES 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 K042131.

When did PROMEDICAL SURGICAL DRAPES receive FDA 510(k) clearance?

PROMEDICAL SURGICAL DRAPES received FDA 510(k) clearance on 2004-12-10, under 510(k) number K042131.

Who is the listed applicant for PROMEDICAL SURGICAL DRAPES?

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 DRAPES?

The FDA product code for PROMEDICAL SURGICAL DRAPES is KKX.

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: KKX)

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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