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FDA 510(k)

TOWEL PACK

K-Number: K952759 · 1995-09-29

ApplicantMedcare Custom Packaging, Inc.
Decision Date1995-09-29
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TOWEL PACK is the device name listed in this FDA 510(k) record. The listed applicant is Medcare Custom Packaging, Inc.. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K952759. 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 TOWEL PACK?

TOWEL PACK is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Medcare Custom Packaging, Inc.. The 510(k) number is K952759.

When did TOWEL PACK receive FDA 510(k) clearance?

TOWEL PACK received FDA 510(k) clearance on 1995-09-29, under 510(k) number K952759.

Who is the listed applicant for TOWEL PACK?

The FDA 510(k) record lists Medcare Custom Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOWEL PACK?

The FDA product code for TOWEL PACK is KKX.

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Other records listing Medcare Custom Packaging, 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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