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FDA 510(k)

SYSTEM, ECHO, PULSED ULTRASONIC DIAG.

K-Number: K802708 · 1981-01-07

ApplicantGeneral Electric Co.
Decision Date1981-01-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYSTEM, ECHO, PULSED ULTRASONIC DIAG. is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802708. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEM, ECHO, PULSED ULTRASONIC DIAG.?

SYSTEM, ECHO, PULSED ULTRASONIC DIAG. is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is General Electric Co.. The 510(k) number is K802708.

When did SYSTEM, ECHO, PULSED ULTRASONIC DIAG. receive FDA 510(k) clearance?

SYSTEM, ECHO, PULSED ULTRASONIC DIAG. received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802708.

Who is the listed applicant for SYSTEM, ECHO, PULSED ULTRASONIC DIAG.?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYSTEM, ECHO, PULSED ULTRASONIC DIAG.?

The FDA product code for SYSTEM, ECHO, PULSED ULTRASONIC DIAG. is IYO.

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Other records listing General Electric Co. 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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