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FDA 510(k)

RPS-50 BEAM SCANNER

K-Number: K962080 · 1996-08-23

ApplicantSofield Science Services, Inc.
Decision Date1996-08-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RPS-50 BEAM SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Sofield Science Services, Inc.. It received FDA 510(k) clearance on 1996-08-23 under 510(k) number K962080. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RPS-50 BEAM SCANNER?

RPS-50 BEAM SCANNER is a medical device that received FDA 510(k) clearance on 1996-08-23. The listed applicant is Sofield Science Services, Inc.. The 510(k) number is K962080.

When did RPS-50 BEAM SCANNER receive FDA 510(k) clearance?

RPS-50 BEAM SCANNER received FDA 510(k) clearance on 1996-08-23, under 510(k) number K962080.

Who is the listed applicant for RPS-50 BEAM SCANNER?

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

What is the FDA product code for RPS-50 BEAM SCANNER?

The FDA product code for RPS-50 BEAM SCANNER is IYE.

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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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