ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI.
K-Number: K780141 · 1978-03-09
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Device Summary
Frequently Asked Questions
What is the ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI.?
ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI. is a medical device that received FDA 510(k) clearance on 1978-03-09. The listed applicant is Harleco. The 510(k) number is K780141.
When did ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI. receive FDA 510(k) clearance?
ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI. received FDA 510(k) clearance on 1978-03-09, under 510(k) number K780141.
Who is the listed applicant for ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI.?
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 ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI.?
The FDA product code for ULTRAZYME PLUS AMYL, CENTRIFICHEM APPLI. is CIJ.
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: CIJ)
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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