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FDA 510(k)

STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400

K-Number: K860447 · 1986-02-19

Decision Date1986-02-19
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400 is the device name listed in this FDA 510(k) record. The listed applicant is Standard Textile Co., Inc.. It received FDA 510(k) clearance on 1986-02-19 under 510(k) number K860447. 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 STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400?

STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400 is a medical device that received FDA 510(k) clearance on 1986-02-19. The listed applicant is Standard Textile Co., Inc.. The 510(k) number is K860447.

When did STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400 receive FDA 510(k) clearance?

STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400 received FDA 510(k) clearance on 1986-02-19, under 510(k) number K860447.

Who is the listed applicant for STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400?

The FDA 510(k) record lists Standard Textile Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400?

The FDA product code for STANGUARD O.R. TOWEL PACK-4TOWEL PACK #278220400 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 Standard Textile Co., 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.

View all 23 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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