510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K905497Substantially Equivalent

Master Flow i.v. Pumpette

The Master Medical Corp., San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905497 is the FDA 510(k) clearance record for MASTER FLOW I.V. PUMPETTE, a class II device, cleared for The Master Medical Corp. on under FDA product code LDR (Controller, Infusion, Intravascular, Electronic). FDA records list 6 510(k) clearances for The Master Medical Corp., from to . As of , FDA records show no recalls naming K905497.

Clearance record

Decision date
Received
(130 days to decision)
Product code
LDR Controller, Infusion, Intravascular, Electronic
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
The Master Medical Corp. 201 Spear St., San Francisco CA
Third party review
No

Clearances, product code LDR

Trailing 12 months

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

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