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FDA 510(k)

DOSIMETRIC RELEASE OF GAMMA RADIATION

K-Number: K832211 · 1983-09-29

ApplicantKirschner Medical Corp.
Decision Date1983-09-29
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DOSIMETRIC RELEASE OF GAMMA RADIATION is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832211. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSIMETRIC RELEASE OF GAMMA RADIATION?

DOSIMETRIC RELEASE OF GAMMA RADIATION is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K832211.

When did DOSIMETRIC RELEASE OF GAMMA RADIATION receive FDA 510(k) clearance?

DOSIMETRIC RELEASE OF GAMMA RADIATION received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832211.

Who is the listed applicant for DOSIMETRIC RELEASE OF GAMMA RADIATION?

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

What is the FDA product code for DOSIMETRIC RELEASE OF GAMMA RADIATION?

The FDA product code for DOSIMETRIC RELEASE OF GAMMA RADIATION is JDI.

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Other records listing Kirschner Medical Corp. as applicant

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Related Devices (Code: JDI)

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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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