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FDA 510(k)

VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM

K-Number: K873546 · 1988-01-29

ApplicantReimers Engineering, Inc.
Decision Date1988-01-29
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Reimers Engineering, Inc.. It received FDA 510(k) clearance on 1988-01-29 under 510(k) number K873546. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM?

VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Reimers Engineering, Inc.. The 510(k) number is K873546.

When did VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM receive FDA 510(k) clearance?

VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM received FDA 510(k) clearance on 1988-01-29, under 510(k) number K873546.

Who is the listed applicant for VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM?

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

What is the FDA product code for VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM?

The FDA product code for VES-TEMP MODEL VT1 MONOPLACE COOL/HEAT SYSTEM is DWJ.

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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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