FDA 510(k)

ELMED WMC 10 AND BC 50 M/M

K-Number: K832589 · 1984-04-23

Decision Date1984-04-23

Product Code

DecisionSubstantially Equivalent

Device Summary

ELMED WMC 10 AND BC 50 M/M is the device name listed in this FDA 510(k) record. The listed applicant is Elmed, Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K832589. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELMED WMC 10 AND BC 50 M/M?

ELMED WMC 10 AND BC 50 M/M is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Elmed, Inc.. The 510(k) number is K832589.

When did ELMED WMC 10 AND BC 50 M/M receive FDA 510(k) clearance?

ELMED WMC 10 AND BC 50 M/M received FDA 510(k) clearance on 1984-04-23, under 510(k) number K832589.

Who is the listed applicant for ELMED WMC 10 AND BC 50 M/M?

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

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Other records listing Elmed, Inc. as applicant

K010465DENSTAT K974793ELMED ESU 120 M/M DIGITAL K953271ELMED RF-ALERT K952110ELMED THERMO-FLUX K926517ELMED LBC 50-P K932938ELMED ESU 300 M/M AND DIGITAL

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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.