V-PRIMER
K-Number: K942017 · 1994-07-06
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Device Summary
Frequently Asked Questions
What is the V-PRIMER?
V-PRIMER is a medical device that received FDA 510(k) clearance on 1994-07-06. The listed applicant is Parkell, Inc.. The 510(k) number is K942017.
When did V-PRIMER receive FDA 510(k) clearance?
V-PRIMER received FDA 510(k) clearance on 1994-07-06, under 510(k) number K942017.
Who is the listed applicant for V-PRIMER?
The FDA 510(k) record lists Parkell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for V-PRIMER?
The FDA product code for V-PRIMER is KLE.
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 Parkell, Inc. 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: KLE)
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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