PHASE PLUS
K-Number: K963609 · 1996-11-14
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Device Summary
Frequently Asked Questions
What is the PHASE PLUS?
PHASE PLUS is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Zhermack S.P.A.. The 510(k) number is K963609.
When did PHASE PLUS receive FDA 510(k) clearance?
PHASE PLUS received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963609.
Who is the listed applicant for PHASE PLUS?
The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHASE PLUS?
The FDA product code for PHASE PLUS is ELW.
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 Zhermack S.P.A. 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: ELW)
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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