FDA 510(k)

BEAM LIMITING DEVICE

K-Number: K828605 · 1983-01-03

Decision Date1983-01-03

Product Code

DecisionSubstantially Equivalent

Device Summary

BEAM LIMITING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Rinn Corp.. It received FDA 510(k) clearance on 1983-01-03 under 510(k) number K828605. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAM LIMITING DEVICE?

BEAM LIMITING DEVICE is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Rinn Corp.. The 510(k) number is K828605.

When did BEAM LIMITING DEVICE receive FDA 510(k) clearance?

BEAM LIMITING DEVICE received FDA 510(k) clearance on 1983-01-03, under 510(k) number K828605.

Who is the listed applicant for BEAM LIMITING DEVICE?

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

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Other records listing Rinn Corp. as applicant

K932134RINN UNIVERSAL COLLIMATOR K913885RINN E-Z CAPPER K813378UNI-BITE DENTAL X-RAY FILM HOLDER K772313X-RAY CO-ORDINATOR

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.