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FDA 510(k)

REHCOR

K-Number: K990813 · 1999-04-12

ApplicantElectromed Corp.
Decision Date1999-04-12
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REHCOR is the device name listed in this FDA 510(k) record. The listed applicant is Electromed Corp.. It received FDA 510(k) clearance on 1999-04-12 under 510(k) number K990813. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REHCOR?

REHCOR is a medical device that received FDA 510(k) clearance on 1999-04-12. The listed applicant is Electromed Corp.. The 510(k) number is K990813.

When did REHCOR receive FDA 510(k) clearance?

REHCOR received FDA 510(k) clearance on 1999-04-12, under 510(k) number K990813.

Who is the listed applicant for REHCOR?

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

What is the FDA product code for REHCOR?

The FDA product code for REHCOR is ISD.

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Related Devices (Code: ISD)

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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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