CK-1 ULTRAZYME PLUS
K-Number: K771389 · 1977-09-02
Device Summary
Frequently Asked Questions
What is the CK-1 ULTRAZYME PLUS?
CK-1 ULTRAZYME PLUS is a medical device that received FDA 510(k) clearance on 1977-09-02. The listed applicant is Harleco. The 510(k) number is K771389.
When did CK-1 ULTRAZYME PLUS receive FDA 510(k) clearance?
CK-1 ULTRAZYME PLUS received FDA 510(k) clearance on 1977-09-02, under 510(k) number K771389.
Who is the listed applicant for CK-1 ULTRAZYME PLUS?
The FDA 510(k) record lists Harleco as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CK-1 ULTRAZYME PLUS?
The FDA product code for CK-1 ULTRAZYME PLUS is CGS.
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 Harleco 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: CGS)
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.