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FDA 510(k)

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE

K-Number: K880714 · 1988-04-21

ApplicantDiasonics, Inc.
Decision Date1988-04-21
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K880714. 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 DIASONICS QT ENDORECTAL 7.5 MHZ PROBE?

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Diasonics, Inc.. The 510(k) number is K880714.

When did DIASONICS QT ENDORECTAL 7.5 MHZ PROBE receive FDA 510(k) clearance?

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE received FDA 510(k) clearance on 1988-04-21, under 510(k) number K880714.

Who is the listed applicant for DIASONICS QT ENDORECTAL 7.5 MHZ PROBE?

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

What is the FDA product code for DIASONICS QT ENDORECTAL 7.5 MHZ PROBE?

The FDA product code for DIASONICS QT ENDORECTAL 7.5 MHZ PROBE is IYO.

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Other records listing Diasonics, 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.

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Related Devices (Code: IYO)

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.

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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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