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FDA 510(k)

VENAPULSE MODELS VP-25 AND VP-50

K-Number: K903894 · 1991-04-03

Decision Date1991-04-03
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENAPULSE MODELS VP-25 AND VP-50 is the device name listed in this FDA 510(k) record. The listed applicant is Aci Medical, Inc.. It received FDA 510(k) clearance on 1991-04-03 under 510(k) number K903894. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENAPULSE MODELS VP-25 AND VP-50?

VENAPULSE MODELS VP-25 AND VP-50 is a medical device that received FDA 510(k) clearance on 1991-04-03. The listed applicant is Aci Medical, Inc.. The 510(k) number is K903894.

When did VENAPULSE MODELS VP-25 AND VP-50 receive FDA 510(k) clearance?

VENAPULSE MODELS VP-25 AND VP-50 received FDA 510(k) clearance on 1991-04-03, under 510(k) number K903894.

Who is the listed applicant for VENAPULSE MODELS VP-25 AND VP-50?

The FDA 510(k) record lists Aci Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENAPULSE MODELS VP-25 AND VP-50?

The FDA product code for VENAPULSE MODELS VP-25 AND VP-50 is JOW.

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 Aci Medical, 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: JOW)

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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