510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K852674Substantially Equivalent

Stryker 988 ICU Bed

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

K852674 is the FDA 510(k) clearance record for STRYKER 988 ICU BED, a class II device, cleared for Stryker Corp. on under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show no recalls naming K852674.

Clearance record

Decision date
Received
(22 days to decision)
Product code
FNL Bed, Ac-Powered Adjustable Hospital
Regulation
21 CFR 880.5100
Device class
Class II
Review panel
General Hospital
Applicant
Stryker Corp. 420 Alcott St., Kalamazoo MI
Third party review
No

Clearances, product code FNL

Trailing 12 months

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

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