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FDA 510(k)

CK 4900 SERIES, GOWN AND TOWEL PAK

K-Number: K874760 · 1987-12-10

Decision Date1987-12-10
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CK 4900 SERIES, GOWN AND TOWEL PAK 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 1987-12-10 under 510(k) number K874760. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CK 4900 SERIES, GOWN AND TOWEL PAK?

CK 4900 SERIES, GOWN AND TOWEL PAK is a medical device that received FDA 510(k) clearance on 1987-12-10. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K874760.

When did CK 4900 SERIES, GOWN AND TOWEL PAK receive FDA 510(k) clearance?

CK 4900 SERIES, GOWN AND TOWEL PAK received FDA 510(k) clearance on 1987-12-10, under 510(k) number K874760.

Who is the listed applicant for CK 4900 SERIES, GOWN AND TOWEL PAK?

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 4900 SERIES, GOWN AND TOWEL PAK?

The FDA product code for CK 4900 SERIES, GOWN AND TOWEL PAK is LRO.

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.

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.

View all 10 devices →

Related Devices (Code: LRO)

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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