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FDA 510(k)

V-PRIMER

K-Number: K942017 · 1994-07-06

ApplicantParkell, Inc.
Decision Date1994-07-06
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

V-PRIMER is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 1994-07-06 under 510(k) number K942017. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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