FDA 510(k)

VITATRON M

K-Number: K852034 · 1986-01-03

Decision Date1986-01-03

Product Code

DecisionSubstantially Equivalent

Device Summary

VITATRON 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 1986-01-03 under 510(k) number K852034. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITATRON M?

VITATRON M is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is Elmed, Inc.. The 510(k) number is K852034.

When did VITATRON M receive FDA 510(k) clearance?

VITATRON M received FDA 510(k) clearance on 1986-01-03, under 510(k) number K852034.

Who is the listed applicant for VITATRON M?

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

Related Clinical Trials

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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.