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FDA 510(k)

OR TOWEL PACKS

K-Number: K894764 · 1989-08-18

ApplicantAdvance Medical Designs, Inc.
Decision Date1989-08-18
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OR TOWEL PACKS is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1989-08-18 under 510(k) number K894764. 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 OR TOWEL PACKS?

OR TOWEL PACKS is a medical device that received FDA 510(k) clearance on 1989-08-18. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K894764.

When did OR TOWEL PACKS receive FDA 510(k) clearance?

OR TOWEL PACKS received FDA 510(k) clearance on 1989-08-18, under 510(k) number K894764.

Who is the listed applicant for OR TOWEL PACKS?

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

What is the FDA product code for OR TOWEL PACKS?

The FDA product code for OR TOWEL PACKS is KKX.

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Other records listing Advance Medical Designs, 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.

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Related Devices (Code: KKX)

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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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