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FDA 510(k)

HALE SUN SURGICAL TOWEL OR O.R. TOWEL

K-Number: K905803 · 1991-05-21

ApplicantHale Sun Industries, Ltd.
Decision Date1991-05-21
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HALE SUN SURGICAL TOWEL OR O.R. TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Hale Sun Industries, Ltd.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K905803. 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 HALE SUN SURGICAL TOWEL OR O.R. TOWEL?

HALE SUN SURGICAL TOWEL OR O.R. TOWEL is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Hale Sun Industries, Ltd.. The 510(k) number is K905803.

When did HALE SUN SURGICAL TOWEL OR O.R. TOWEL receive FDA 510(k) clearance?

HALE SUN SURGICAL TOWEL OR O.R. TOWEL received FDA 510(k) clearance on 1991-05-21, under 510(k) number K905803.

Who is the listed applicant for HALE SUN SURGICAL TOWEL OR O.R. TOWEL?

The FDA 510(k) record lists Hale Sun Industries, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HALE SUN SURGICAL TOWEL OR O.R. TOWEL?

The FDA product code for HALE SUN SURGICAL TOWEL OR O.R. TOWEL is KKX.

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Related Devices (Code: KKX)

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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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