FDA 510(k)

TELHTHERAPY SIMULATOR AECL-CP, G-3200

K-Number: K771096 · 1977-07-01

Decision Date1977-07-01

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

TELHTHERAPY SIMULATOR AECL-CP, G-3200 is the device name listed in this FDA 510(k) record. The listed applicant is Atomic Energy of Canada. It received FDA 510(k) clearance on 1977-07-01 under 510(k) number K771096. 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 TELHTHERAPY SIMULATOR AECL-CP, G-3200?

TELHTHERAPY SIMULATOR AECL-CP, G-3200 is a medical device that received FDA 510(k) clearance on 1977-07-01. The listed applicant is Atomic Energy of Canada. The 510(k) number is K771096.

When did TELHTHERAPY SIMULATOR AECL-CP, G-3200 receive FDA 510(k) clearance?

TELHTHERAPY SIMULATOR AECL-CP, G-3200 received FDA 510(k) clearance on 1977-07-01, under 510(k) number K771096.

Who is the listed applicant for TELHTHERAPY SIMULATOR AECL-CP, G-3200?

The FDA 510(k) record lists Atomic Energy of Canada as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELHTHERAPY SIMULATOR AECL-CP, G-3200?

The FDA product code for TELHTHERAPY SIMULATOR AECL-CP, G-3200 is JAA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.