FDA 510(k)

VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000

K-Number: K984270 · 1999-05-20

Decision Date1999-05-20

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Roger L. Goodman, D.D.S., P.C.. It received FDA 510(k) clearance on 1999-05-20 under 510(k) number K984270. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000?

VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000 is a medical device that received FDA 510(k) clearance on 1999-05-20. The listed applicant is Roger L. Goodman, D.D.S., P.C.. The 510(k) number is K984270.

When did VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000 receive FDA 510(k) clearance?

VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000 received FDA 510(k) clearance on 1999-05-20, under 510(k) number K984270.

Who is the listed applicant for VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000?

The FDA 510(k) record lists Roger L. Goodman, D.D.S., P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000?

The FDA product code for VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000 is MED.

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Official Source

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