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FDA 510(k)

CK 1600 SERIES, TOWELS

K-Number: K872395 · 1987-07-02

ApplicantCurrie Medical Specialties, Inc.
Decision Date1987-07-02
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CK 1600 SERIES, TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Currie Medical Specialties, Inc.. It received FDA 510(k) clearance on 1987-07-02 under 510(k) number K872395. 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 CK 1600 SERIES, TOWELS?

CK 1600 SERIES, TOWELS is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K872395.

When did CK 1600 SERIES, TOWELS receive FDA 510(k) clearance?

CK 1600 SERIES, TOWELS received FDA 510(k) clearance on 1987-07-02, under 510(k) number K872395.

Who is the listed applicant for CK 1600 SERIES, TOWELS?

The FDA 510(k) record lists Currie Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CK 1600 SERIES, TOWELS?

The FDA product code for CK 1600 SERIES, TOWELS is KKX.

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Other records listing Currie Medical Specialties, 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.

K112311ALP 501 RB PUMP SYSTEMK902441DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)K874760CK 4900 SERIES, GOWN AND TOWEL PAKK871737CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTORK864816CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGEK864697CK 6000 SERIES, TOWELS

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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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