FDA 510(k)

ELECTRONIC PHOTOSPOT 20

K-Number: K922240 · 1992-08-07

ApplicantToshiba America Medical Systems, In.C

Decision Date1992-08-07

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ELECTRONIC PHOTOSPOT 20 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 1992-08-07 under 510(k) number K922240. 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 ELECTRONIC PHOTOSPOT 20?

ELECTRONIC PHOTOSPOT 20 is a medical device that received FDA 510(k) clearance on 1992-08-07. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K922240.

When did ELECTRONIC PHOTOSPOT 20 receive FDA 510(k) clearance?

ELECTRONIC PHOTOSPOT 20 received FDA 510(k) clearance on 1992-08-07, under 510(k) number K922240.

Who is the listed applicant for ELECTRONIC PHOTOSPOT 20?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC PHOTOSPOT 20?

The FDA product code for ELECTRONIC PHOTOSPOT 20 is 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.