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FDA 510(k)

TECH DYNE - HP-2000, SKREEN TEST, RMS-200

K-Number: K920183 · 1992-06-15

ApplicantTech Dyne Group
Decision Date1992-06-15
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECH DYNE - HP-2000, SKREEN TEST, RMS-200 is the device name listed in this FDA 510(k) record. The listed applicant is Tech Dyne Group. It received FDA 510(k) clearance on 1992-06-15 under 510(k) number K920183. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECH DYNE - HP-2000, SKREEN TEST, RMS-200?

TECH DYNE - HP-2000, SKREEN TEST, RMS-200 is a medical device that received FDA 510(k) clearance on 1992-06-15. The listed applicant is Tech Dyne Group. The 510(k) number is K920183.

When did TECH DYNE - HP-2000, SKREEN TEST, RMS-200 receive FDA 510(k) clearance?

TECH DYNE - HP-2000, SKREEN TEST, RMS-200 received FDA 510(k) clearance on 1992-06-15, under 510(k) number K920183.

Who is the listed applicant for TECH DYNE - HP-2000, SKREEN TEST, RMS-200?

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

What is the FDA product code for TECH DYNE - HP-2000, SKREEN TEST, RMS-200?

The FDA product code for TECH DYNE - HP-2000, SKREEN TEST, RMS-200 is LBB.

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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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