510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K984270Substantially Equivalent

Vapo-Solution for Use in Mdt Harvey Chemiclave Sterilizers, Models 5000, 5500, and 6000

Roger L. Goodman, D.D.S., P.C., Mason MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K984270 is the FDA 510(k) clearance record for VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000, a class II device, cleared for Roger L. Goodman, D.D.S., P.C. on under FDA product code MED (Sterilant, Medical Devices). FDA records list one 510(k) clearance for Roger L. Goodman, D.D.S., P.C. As of , FDA records show no recalls naming K984270.

Clearance record

Decision date
Received
(171 days to decision)
Product code
MED Sterilant, Medical Devices
Regulation
21 CFR 880.6885
Device class
Class II
Review panel
General Hospital
Applicant
Roger L. Goodman, D.D.S., P.C. 200 Temple St., Mason MI
510(k) summary
Summary
Third party review
No

Clearances, product code MED

Trailing 12 months
1 clearance under product code MED in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MED, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260