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FDA 510(k)

VOLMED OPERATION DRAPE

K-Number: K955872 · 1996-03-12

Decision Date1996-03-12
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VOLMED OPERATION DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Medal Intl. Sales Co., LLC. It received FDA 510(k) clearance on 1996-03-12 under 510(k) number K955872. 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 VOLMED OPERATION DRAPE?

VOLMED OPERATION DRAPE is a medical device that received FDA 510(k) clearance on 1996-03-12. The listed applicant is Medal Intl. Sales Co., LLC. The 510(k) number is K955872.

When did VOLMED OPERATION DRAPE receive FDA 510(k) clearance?

VOLMED OPERATION DRAPE received FDA 510(k) clearance on 1996-03-12, under 510(k) number K955872.

Who is the listed applicant for VOLMED OPERATION DRAPE?

The FDA 510(k) record lists Medal Intl. Sales Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOLMED OPERATION DRAPE?

The FDA product code for VOLMED OPERATION DRAPE 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.

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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