VACUUM COMPRESSION INJECTOR
K-Number: K851809 · 1985-07-01
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Device Summary
Frequently Asked Questions
What is the VACUUM COMPRESSION INJECTOR?
VACUUM COMPRESSION INJECTOR is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Uci Corp.. The 510(k) number is K851809.
When did VACUUM COMPRESSION INJECTOR receive FDA 510(k) clearance?
VACUUM COMPRESSION INJECTOR received FDA 510(k) clearance on 1985-07-01, under 510(k) number K851809.
Who is the listed applicant for VACUUM COMPRESSION INJECTOR?
The FDA 510(k) record lists Uci Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VACUUM COMPRESSION INJECTOR?
The FDA product code for VACUUM COMPRESSION INJECTOR is KZE.
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.
Related Devices (Code: KZE)
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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