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FDA 510(k)

BEAM BLOCK SHAPER

K-Number: K837344 · 1983-05-09

Decision Date1983-05-09
Product Code
DecisionSubstantially Equivalent

Device Summary

BEAM BLOCK SHAPER is the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K837344. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAM BLOCK SHAPER?

BEAM BLOCK SHAPER is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K837344.

When did BEAM BLOCK SHAPER receive FDA 510(k) clearance?

BEAM BLOCK SHAPER received FDA 510(k) clearance on 1983-05-09, under 510(k) number K837344.

Who is the listed applicant for BEAM BLOCK SHAPER?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Mick Radio-Nuclear Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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