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FDA 510(k)

SURGICAL TOWELS

K-Number: K851407 · 1985-06-07

ApplicantDiack
Decision Date1985-06-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Diack. It received FDA 510(k) clearance on 1985-06-07 under 510(k) number K851407. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL TOWELS?

SURGICAL TOWELS is a medical device that received FDA 510(k) clearance on 1985-06-07. The listed applicant is Diack. The 510(k) number is K851407.

When did SURGICAL TOWELS receive FDA 510(k) clearance?

SURGICAL TOWELS received FDA 510(k) clearance on 1985-06-07, under 510(k) number K851407.

Who is the listed applicant for SURGICAL TOWELS?

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

What is the FDA product code for SURGICAL TOWELS?

The FDA product code for SURGICAL TOWELS is JOJ.

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.

Related Devices (Code: JOJ)

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

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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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