510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912346Substantially Equivalent

Medikeeper

Medikeeper, Inc., Philadelphia PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912346 is the FDA 510(k) clearance record for MEDIKEEPER, a class I device, cleared for Medikeeper, Inc. on under FDA product code BRY (Cabinet, Table And Tray, Anesthesia). FDA records list one 510(k) clearance for Medikeeper, Inc. As of , FDA records show no recalls naming K912346.

Clearance record

Decision date
Received
(63 days to decision)
Product code
BRY Cabinet, Table And Tray, Anesthesia
Regulation
21 CFR 868.6100
Device class
Class I
Review panel
Anesthesiology
Applicant
Medikeeper, Inc. P.O.Box 18692, Philadelphia PA
510(k) summary
Statement
Third party review
No

Clearances, product code BRY

Trailing 12 months

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

FDA records show no clearances under product code BRY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BRY, 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