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FDA 510(k)

VIDA 55 PULSE-ECHO ULTRASONIC DEVICE

K-Number: K802279 · 1980-12-15

ApplicantVida, Inc.
Decision Date1980-12-15
Product CodeEWG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VIDA 55 PULSE-ECHO ULTRASONIC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vida, Inc.. It received FDA 510(k) clearance on 1980-12-15 under 510(k) number K802279. The device is classified under product code EWG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDA 55 PULSE-ECHO ULTRASONIC DEVICE?

VIDA 55 PULSE-ECHO ULTRASONIC DEVICE is a medical device that received FDA 510(k) clearance on 1980-12-15. The listed applicant is Vida, Inc.. The 510(k) number is K802279.

When did VIDA 55 PULSE-ECHO ULTRASONIC DEVICE receive FDA 510(k) clearance?

VIDA 55 PULSE-ECHO ULTRASONIC DEVICE received FDA 510(k) clearance on 1980-12-15, under 510(k) number K802279.

Who is the listed applicant for VIDA 55 PULSE-ECHO ULTRASONIC DEVICE?

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

What is the FDA product code for VIDA 55 PULSE-ECHO ULTRASONIC DEVICE?

The FDA product code for VIDA 55 PULSE-ECHO ULTRASONIC DEVICE is EWG.

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: EWG)

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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