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FDA 510(k)

OPERATION ROOM TOWEL

K-Number: K881479 · 1988-04-14

ApplicantRahn Laboratories
Decision Date1988-04-14
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATION ROOM TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Rahn Laboratories. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K881479. 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 OPERATION ROOM TOWEL?

OPERATION ROOM TOWEL is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Rahn Laboratories. The 510(k) number is K881479.

When did OPERATION ROOM TOWEL receive FDA 510(k) clearance?

OPERATION ROOM TOWEL received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881479.

Who is the listed applicant for OPERATION ROOM TOWEL?

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

What is the FDA product code for OPERATION ROOM TOWEL?

The FDA product code for OPERATION ROOM TOWEL is KKX.

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Other records listing Rahn Laboratories as applicant

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Related Devices (Code: KKX)

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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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