MICROSTAR VC1 VOLUMETRIC CYCLER
K-Number: K832141 · 1983-10-14
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Device Summary
Frequently Asked Questions
What is the MICROSTAR VC1 VOLUMETRIC CYCLER?
MICROSTAR VC1 VOLUMETRIC CYCLER is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Medionics International , Ltd.. The 510(k) number is K832141.
When did MICROSTAR VC1 VOLUMETRIC CYCLER receive FDA 510(k) clearance?
MICROSTAR VC1 VOLUMETRIC CYCLER received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832141.
Who is the listed applicant for MICROSTAR VC1 VOLUMETRIC CYCLER?
The FDA 510(k) record lists Medionics International , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSTAR VC1 VOLUMETRIC CYCLER?
The FDA product code for MICROSTAR VC1 VOLUMETRIC CYCLER is FKX.
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 Medionics International , Ltd. 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: FKX)
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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