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FDA 510(k)

360 DEG. ROTATING 1/2 BEAM BLOCK

K-Number: K941719 · 1994-07-18

ApplicantMedtec, Inc.
Decision Date1994-07-18
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

360 DEG. ROTATING 1/2 BEAM BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1994-07-18 under 510(k) number K941719. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 360 DEG. ROTATING 1/2 BEAM BLOCK?

360 DEG. ROTATING 1/2 BEAM BLOCK is a medical device that received FDA 510(k) clearance on 1994-07-18. The listed applicant is Medtec, Inc.. The 510(k) number is K941719.

When did 360 DEG. ROTATING 1/2 BEAM BLOCK receive FDA 510(k) clearance?

360 DEG. ROTATING 1/2 BEAM BLOCK received FDA 510(k) clearance on 1994-07-18, under 510(k) number K941719.

Who is the listed applicant for 360 DEG. ROTATING 1/2 BEAM BLOCK?

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

What is the FDA product code for 360 DEG. ROTATING 1/2 BEAM BLOCK?

The FDA product code for 360 DEG. ROTATING 1/2 BEAM BLOCK is IXI.

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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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