510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K874060Substantially Equivalent

Converta-Litter

Camtec, Cambridge MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874060 is the FDA 510(k) clearance record for CONVERTA-LITTER, a class I device, cleared for Camtec on under FDA product code INN (Chair, Adjustable, Mechanical). FDA records list 2 510(k) clearances for Camtec, from to . As of , FDA records show no recalls naming K874060.

Clearance record

Decision date
Received
(66 days to decision)
Product code
INN Chair, Adjustable, Mechanical
Regulation
21 CFR 890.3100
Device class
Class I
Review panel
Physical Medicine
Applicant
Camtec 300 Muir St., Cambridge MD
Third party review
No

Clearances, product code INN

Trailing 12 months

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

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