Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K930915Substantially Equivalent

Fluori Methane Ss- a Vapocoolant/skin Ref. Device

Gebauer Co, Washington DC / Traditional, Substantially Equivalent

K930915 is the FDA 510(k) clearance record for FLUORI METHANE SS- A VAPOCOOLANT/SKIN REF. DEVICE, cleared for Gebauer Co. on under FDA product code MLY (Vapocoolant Device). FDA records list 10 510(k) clearances for Gebauer Co., from to . As of , FDA records show no recalls naming K930915.

Clearance record

Decision date
Received
(583 days to decision)
Product code
MLY Vapocoolant Device
Device class
Unclassified
Review panel
Unknown
Applicant
Gebauer Co. 1920 N. St. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code MLY

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