PLUME MASTER
K-Number: K913036 · 1991-09-06
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Device Summary
Frequently Asked Questions
What is the PLUME MASTER?
PLUME MASTER is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Sorex Medical. The 510(k) number is K913036.
When did PLUME MASTER receive FDA 510(k) clearance?
PLUME MASTER received FDA 510(k) clearance on 1991-09-06, under 510(k) number K913036.
Who is the listed applicant for PLUME MASTER?
The FDA 510(k) record lists Sorex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLUME MASTER?
The FDA product code for PLUME MASTER is FYD.
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 Sorex Medical 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: FYD)
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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