510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912237Substantially Equivalent

Stryker Eclipse Warming Stretcher

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

K912237 is the FDA 510(k) clearance record for STRYKER ECLIPSE WARMING STRETCHER, a class I device, cleared for Stryker Medical on under FDA product code DWI (Saw, Electrically Powered). FDA records list 14 510(k) clearances for Stryker Medical, from to . As of , FDA records show no recalls naming K912237.

Clearance record

Decision date
Received
(70 days to decision)
Product code
DWI Saw, Electrically Powered
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Stryker Medical 6300 S. Sprinkle Rd., Kalamazoo MI
510(k) summary
Statement
Third party review
No

Clearances, product code DWI

Trailing 12 months

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

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