CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR
K-Number: K871737 · 1987-06-22
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Device Summary
Frequently Asked Questions
What is the CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR?
CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR is a medical device that received FDA 510(k) clearance on 1987-06-22. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K871737.
When did CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR receive FDA 510(k) clearance?
CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR received FDA 510(k) clearance on 1987-06-22, under 510(k) number K871737.
Who is the listed applicant for CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR?
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 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR?
The FDA product code for CK 7000 SERIES 5 IN 1 CONNECTOR AND Y-CONNECTOR is BZA.
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.
Related Devices (Code: BZA)
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
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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