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FDA 510(k)

CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE

K-Number: K864816 · 1987-01-08

ApplicantCurrie Medical Specialties, Inc.
Decision Date1987-01-08
Product Code
DecisionSubstantially Equivalent

Device Summary

CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE 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 1987-01-08 under 510(k) number K864816. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE?

CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE is a medical device that received FDA 510(k) clearance on 1987-01-08. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K864816.

When did CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE receive FDA 510(k) clearance?

CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE received FDA 510(k) clearance on 1987-01-08, under 510(k) number K864816.

Who is the listed applicant for CK 5000 SERIES, ACE BANDAGE/ESMARK BANDAGE?

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

Related Clinical Trials

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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 PAKK872395CK 1600 SERIES, TOWELSK871737CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTORK864697CK 6000 SERIES, TOWELS

View all 10 devices →

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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