Skip to content

Torrent 00711579

by US Endoscopy 2 variants

Torrent 00711579 is a Class II device made by US Endoscopy, cleared under FDA 510(k) K882048 on 31 Oct 1988 and listed in FDA GUDID since 1 Apr 2020 (UDI-DI 00724995180522), 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) K882048

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 Number00724995180522 UDI-DI Date1 Apr 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK882048 Date31 Oct 1988DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K882048 decided 31 Oct 1988 Active
  • FDA GUDID UDI-DI 00724995180522 listed 1 Apr 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K882048
  2. Listed FDA GUDID 00724995180522

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Torrent
Generic name
Surgical irrigation pump
Model / Ref / Catalog
00711579
Primary DI / UDI-DI
00724995180522
510(k) Number
FDA product code
KNS
GMDN term
Surgical irrigation pump
Device class
Class II
Regulation number
876.4300
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNS (Unit, electrosurgical, endoscopic (with or without accessories)).

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)