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FDA 510(k)

HUCK TOWEL

K-Number: K852945 · 1985-07-29

ApplicantSouth Mountain Medical
Decision Date1985-07-29
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HUCK TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is South Mountain Medical. It received FDA 510(k) clearance on 1985-07-29 under 510(k) number K852945. 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 HUCK TOWEL?

HUCK TOWEL is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is South Mountain Medical. The 510(k) number is K852945.

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

HUCK TOWEL received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852945.

Who is the listed applicant for HUCK TOWEL?

The FDA 510(k) record lists South Mountain Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUCK TOWEL?

The FDA product code for HUCK TOWEL is KKX.

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Other records listing South Mountain Medical 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.

K853742GAUZE SPONGEK851276ACTION PACK831806SUTURE KITS STERILIZED W/GAMA RADIATIONK823485SURE SNIPK812992SURGICAL MASKK811769LAPAROTOMY PADS

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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.

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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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