510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883485Substantially Equivalent

Stryker Pressure Monitor System

Stryker Corp., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883485 is the FDA 510(k) clearance record for STRYKER PRESSURE MONITOR SYSTEM, a class I device, cleared for Stryker Corp. on under FDA product code FTY (Tape, Measuring, Rulers And Calipers). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show no recalls naming K883485.

Clearance record

Decision date
Received
(28 days to decision)
Product code
FTY Tape, Measuring, Rulers And Calipers
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Stryker Corp. 420 Alcott St., Kalamazoo MI
Third party review
No

Clearances, product code FTY

Trailing 12 months

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

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