Adview 9000TP

by American Diagnostic Corporation

Adview 9000TP is a Class II device made by American Diagnostic Corporation, cleared under FDA 510(k) K070750 on 2 May 2007 and listed in FDA GUDID since 31 Jul 2018 (UDI-DI 00634782564650), 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

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00634782564650 UDI-DI	Date31 Jul 2018Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated	NumberK070750	Date2 May 2007Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00634782564650
FDA 510(k) database 510(k) number K070750

Across registries

2 registries list this device

FDA 510(k) K070750 decided 2 May 2007 Active
FDA GUDID UDI-DI 00634782564650 listed 31 Jul 2018 Listed

Timeline

2 dated events

2 May 2007 Cleared FDA 510(k) K070750
31 Jul 2018 Listed FDA GUDID 00634782564650

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Adview
Generic name: Electronic thermometer probe cover
Model / Ref / Catalog: 9000TP

Primary DI / UDI-DI: 00634782564650
510(k) Number: K070750
FDA product code: FLL
GMDN term: Electronic thermometer probe cover

Device class: Class II
Regulation number: 880.2910
GUDID distribution status: In Commercial Distribution

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Properties

Contains latex
Prescription use
Lot / batch number

Other properties (12, all answered No)