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FDA 510(k)

ADMS MULTIPLANE RECTAL PROBE

K-Number: K895359 · 1989-11-22

ApplicantAvalon Technology Corp.
Decision Date1989-11-22
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADMS MULTIPLANE RECTAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Avalon Technology Corp.. It received FDA 510(k) clearance on 1989-11-22 under 510(k) number K895359. 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 MULTIPLANE RECTAL PROBE?

ADMS MULTIPLANE RECTAL PROBE is a medical device that received FDA 510(k) clearance on 1989-11-22. The listed applicant is Avalon Technology Corp.. The 510(k) number is K895359.

When did ADMS MULTIPLANE RECTAL PROBE receive FDA 510(k) clearance?

ADMS MULTIPLANE RECTAL PROBE received FDA 510(k) clearance on 1989-11-22, under 510(k) number K895359.

Who is the listed applicant for ADMS MULTIPLANE RECTAL PROBE?

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

What is the FDA product code for ADMS MULTIPLANE RECTAL PROBE?

The FDA product code for ADMS MULTIPLANE RECTAL PROBE is ITX.

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Other records listing Avalon Technology Corp. 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.

K904317AVALON GENERAL PURPOSE SCANNER, PREVIEW GP

Related Devices (Code: ITX)

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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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