510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K911264Substantially Equivalent

Calibration Kit

S & W Medico Teknik, Denmark, DK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911264 is the FDA 510(k) clearance record for CALIBRATION KIT, a class I device, cleared for S & W Medico Teknik on under FDA product code BXK (Gas, Calibration (Specified Concentration)). FDA records list 49 510(k) clearances for S & W Medico Teknik, from to . As of , FDA records show no recalls naming K911264.

Clearance record

Decision date
Received
(144 days to decision)
Product code
BXK Gas, Calibration (Specified Concentration)
Regulation
21 CFR 868.6400
Device class
Class I
Review panel
Anesthesiology
Applicant
S & W Medico Teknik Herstedvang 8, Denmark, DK
Third party review
No

Clearances, product code BXK

Trailing 12 months

FDA records hold no clearances under product code BXK in the trailing twelve months.

FDA records show no clearances under product code BXK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BXK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260