BEAM BLOCK SHAPER
K-Number: K837344 · 1983-05-09
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Device Summary
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.
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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