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Ritus 8810805001

by Mozarc Medical US LLC

Ritus 8810805001 is a Class II device made by Mozarc Medical US LLC, cleared under FDA 510(k) K780449 on 16 May 1978 and listed in FDA GUDID since 20 Apr 2026 (UDI-DI 10884521811270), 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) K780449

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 Number10884521811270 UDI-DI Date20 Apr 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK780449 Date16 May 1978DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K780449 decided 16 May 1978 Active
  • FDA GUDID UDI-DI 10884521811270 listed 20 Apr 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K780449
  2. Listed FDA GUDID 10884521811270

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Ritus
Generic name
Medical tubing clip/clamp, temporary, non-calibrated, single-use
Model / reference
8810805001
Primary DI / UDI-DI
10884521811270
510(k) Number
FDA product code
FJS
GMDN term
Medical tubing clip/clamp, temporary, non-calibrated, single-use
Device class
Class II
Regulation number
876.5630
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FJS (CATHETER, PERITONEAL, LONG-TERM INDWELLING).

Other devices from Mozarc Medical US LLC

See all devices from Mozarc Medical US LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)