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
K220742Substantially Equivalent

NxtGen Infant Transport Incubator

International Biomedical, Ltd., Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220742 is the FDA 510(k) clearance record for NxtGen Infant Transport Incubator, a class II device, cleared for International Biomedical on under FDA product code FPL (Incubator, Neonatal Transport). FDA records list 17 510(k) clearances for International Biomedical, from to . As of , FDA records show no recalls naming K220742.

Clearance record

Decision date
Received
(123 days to decision)
Product code
FPL Incubator, Neonatal Transport
Regulation
21 CFR 880.5410
Device class
Class II
Review panel
General Hospital
Applicant
International Biomedical 8206 Cross Park Dr., Austin TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FPL

Trailing 12 months

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

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