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Kangaroo 777702E

by Cardinalhealth 2 variants

Kangaroo 777702E is a Class II device made by Cardinalhealth, cleared under FDA 510(k) K042572 on 5 Nov 2004 and listed in FDA GUDID since 31 Jan 2017 (UDI-DI 10884521619678), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K042572

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521619678 UDI-DI Date31 Jan 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK042572 Date5 Nov 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K042572 decided 5 Nov 2004 Active
  • FDA GUDID UDI-DI 10884521619678 listed 31 Jan 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K042572
  2. Listed FDA GUDID 10884521619678

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Kangaroo
Generic name
Exhaled-gas oesophageal intubation detector
Model / Ref / Catalog
777702E
Primary DI / UDI-DI
10884521619678
510(k) Number
FDA product code
KNT
GMDN term
Exhaled-gas oesophageal intubation detector
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNT (TUBES, GASTROINTESTINAL (AND ACCESSORIES)).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)