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FDA 510(k)

DIGITAL FLUROGRAPHIC IMAGING SYSTEM

K-Number: K813217 · 1981-12-29

ApplicantDiasonics, Inc.
Decision Date1981-12-29
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL FLUROGRAPHIC IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813217. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL FLUROGRAPHIC IMAGING SYSTEM?

DIGITAL FLUROGRAPHIC IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Diasonics, Inc.. The 510(k) number is K813217.

When did DIGITAL FLUROGRAPHIC IMAGING SYSTEM receive FDA 510(k) clearance?

DIGITAL FLUROGRAPHIC IMAGING SYSTEM received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813217.

Who is the listed applicant for DIGITAL FLUROGRAPHIC IMAGING SYSTEM?

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 DIGITAL FLUROGRAPHIC IMAGING SYSTEM?

The FDA product code for DIGITAL FLUROGRAPHIC IMAGING SYSTEM is JAA.

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Related Devices (Code: JAA)

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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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