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FDA 510(k)

SURGICAL DRAPES

K-Number: K971159 · 1997-06-24

Decision Date1997-06-24
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is International Medsurg Connection. It received FDA 510(k) clearance on 1997-06-24 under 510(k) number K971159. 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 SURGICAL DRAPES?

SURGICAL DRAPES is a medical device that received FDA 510(k) clearance on 1997-06-24. The listed applicant is International Medsurg Connection. The 510(k) number is K971159.

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

SURGICAL DRAPES received FDA 510(k) clearance on 1997-06-24, under 510(k) number K971159.

Who is the listed applicant for SURGICAL DRAPES?

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

What is the FDA product code for SURGICAL DRAPES?

The FDA product code for 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 International Medsurg Connection 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.

View all 11 devices →

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

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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