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FDA 510(k)

CPA/3.5 MHZ PROBE

K-Number: K911435 · 1992-09-11

ApplicantDiasonics, Inc.
Decision Date1992-09-11
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CPA/3.5 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 1992-09-11 under 510(k) number K911435. 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 CPA/3.5 MHZ PROBE?

CPA/3.5 MHZ PROBE is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Diasonics, Inc.. The 510(k) number is K911435.

When did CPA/3.5 MHZ PROBE receive FDA 510(k) clearance?

CPA/3.5 MHZ PROBE received FDA 510(k) clearance on 1992-09-11, under 510(k) number K911435.

Who is the listed applicant for CPA/3.5 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 CPA/3.5 MHZ PROBE?

The FDA product code for CPA/3.5 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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