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LV-1 Plug 667147-303

by Oscor Inc.

LV-1 Plug 667147-303 is a Class II device made by Oscor Inc., cleared under FDA 510(k) K024156 on 14 Jan 2003 and listed in FDA GUDID since 1 Jun 2026 (UDI-DI 00885672013233), active as of 22 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 22 Oct 2026

Documents

510(k) K024156

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885672013233 UDI-DI Date1 Jun 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK024156 Date14 Jan 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K024156 decided 14 Jan 2003 Active
  • FDA GUDID UDI-DI 00885672013233 listed 1 Jun 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K024156
  2. Listed FDA GUDID 00885672013233

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
LV-1 Plug
Generic name
Implantable pulse generator port plug
Model / Ref / Catalog
667147-303, LV-1 PLUG
Primary DI / UDI-DI
00885672013233
510(k) Number
FDA product code
DTD
GMDN term
Implantable pulse generator port plug
Device class
Class II
Regulation number
870.3620
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K024156)

and 3 more cleared under K024156

Other devices from Oscor Inc.

See all devices from Oscor Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)