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FDA 510(k)

VASOPULSE(TM)/MODEL 5000

K-Number: K863803 · 1987-05-06

ApplicantSonicaid, Inc.
Decision Date1987-05-06
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASOPULSE(TM)/MODEL 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1987-05-06 under 510(k) number K863803. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOPULSE(TM)/MODEL 5000?

VASOPULSE(TM)/MODEL 5000 is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is Sonicaid, Inc.. The 510(k) number is K863803.

When did VASOPULSE(TM)/MODEL 5000 receive FDA 510(k) clearance?

VASOPULSE(TM)/MODEL 5000 received FDA 510(k) clearance on 1987-05-06, under 510(k) number K863803.

Who is the listed applicant for VASOPULSE(TM)/MODEL 5000?

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

What is the FDA product code for VASOPULSE(TM)/MODEL 5000?

The FDA product code for VASOPULSE(TM)/MODEL 5000 is JOM.

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Other records listing Sonicaid, Inc. as applicant

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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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