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FDA 510(k)

ADMS TRANSRECTAL 7.5 MHZ PROBE

K-Number: K870967 · 1987-09-29

ApplicantDiasonics, Inc.
Decision Date1987-09-29
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADMS TRANSRECTAL 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 1987-09-29 under 510(k) number K870967. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADMS TRANSRECTAL 7.5 MHZ PROBE?

ADMS TRANSRECTAL 7.5 MHZ PROBE is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is Diasonics, Inc.. The 510(k) number is K870967.

When did ADMS TRANSRECTAL 7.5 MHZ PROBE receive FDA 510(k) clearance?

ADMS TRANSRECTAL 7.5 MHZ PROBE received FDA 510(k) clearance on 1987-09-29, under 510(k) number K870967.

Who is the listed applicant for ADMS TRANSRECTAL 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 ADMS TRANSRECTAL 7.5 MHZ PROBE?

The FDA product code for ADMS TRANSRECTAL 7.5 MHZ PROBE is ITX.

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Other records listing Diasonics, 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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