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FDA 510(k)

PRO-FECT O.R. TOWEL

K-Number: K882000 · 1988-08-26

ApplicantNetwork Trading Corp.
Decision Date1988-08-26
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRO-FECT O.R. TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Network Trading Corp.. It received FDA 510(k) clearance on 1988-08-26 under 510(k) number K882000. 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 PRO-FECT O.R. TOWEL?

PRO-FECT O.R. TOWEL is a medical device that received FDA 510(k) clearance on 1988-08-26. The listed applicant is Network Trading Corp.. The 510(k) number is K882000.

When did PRO-FECT O.R. TOWEL receive FDA 510(k) clearance?

PRO-FECT O.R. TOWEL received FDA 510(k) clearance on 1988-08-26, under 510(k) number K882000.

Who is the listed applicant for PRO-FECT O.R. TOWEL?

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

What is the FDA product code for PRO-FECT O.R. TOWEL?

The FDA product code for PRO-FECT O.R. TOWEL 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.

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Other records listing Network Trading Corp. 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.

K882021PRO-FECT LAPAROTOMY SPONGESK880535PROFECT SURGEONS' GLOVES

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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