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FDA 510(k)

ROHNAR 7000 DIGITAL DIAGN ULTRASOUND

K-Number: K791505 · 1979-09-17

ApplicantRoche Scientific Corp.
Decision Date1979-09-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ROHNAR 7000 DIGITAL DIAGN ULTRASOUND is the device name listed in this FDA 510(k) record. The listed applicant is Roche Scientific Corp.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791505. 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 ROHNAR 7000 DIGITAL DIAGN ULTRASOUND?

ROHNAR 7000 DIGITAL DIAGN ULTRASOUND is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Roche Scientific Corp.. The 510(k) number is K791505.

When did ROHNAR 7000 DIGITAL DIAGN ULTRASOUND receive FDA 510(k) clearance?

ROHNAR 7000 DIGITAL DIAGN ULTRASOUND received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791505.

Who is the listed applicant for ROHNAR 7000 DIGITAL DIAGN ULTRASOUND?

The FDA 510(k) record lists Roche Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROHNAR 7000 DIGITAL DIAGN ULTRASOUND?

The FDA product code for ROHNAR 7000 DIGITAL DIAGN ULTRASOUND is IYO.

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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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