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FDA 510(k)

REFLEX TREATMENT SYSTEM

K-Number: K994079 · 2000-03-01

ApplicantDeschutes Medical Products, Inc.
Decision Date2000-03-01
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REFLEX TREATMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Deschutes Medical Products, Inc.. It received FDA 510(k) clearance on 2000-03-01 under 510(k) number K994079. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFLEX TREATMENT SYSTEM?

REFLEX TREATMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2000-03-01. The listed applicant is Deschutes Medical Products, Inc.. The 510(k) number is K994079.

When did REFLEX TREATMENT SYSTEM receive FDA 510(k) clearance?

REFLEX TREATMENT SYSTEM received FDA 510(k) clearance on 2000-03-01, under 510(k) number K994079.

Who is the listed applicant for REFLEX TREATMENT SYSTEM?

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

What is the FDA product code for REFLEX TREATMENT SYSTEM?

The FDA product code for REFLEX TREATMENT SYSTEM is HIR.

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Related Devices (Code: HIR)

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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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