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Codman Microsensor® 826633

by Integra LifeSciences Production Corporation

Codman Microsensor® 826633 (82-6633) is a Class II device made by Integra LifeSciences Production Corporation, cleared under FDA 510(k) K991222 on 9 Jul 1999 and listed in FDA GUDID since 1 Apr 2020 (UDI-DI 10381780520436), 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) K991222

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 Number10381780520436 UDI-DI Date1 Apr 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK991222 Date9 Jul 1999DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K991222 decided 9 Jul 1999 Active
  • FDA GUDID UDI-DI 10381780520436 listed 1 Apr 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K991222
  2. Listed FDA GUDID 10381780520436

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Codman Microsensor®
Generic name
Ventricular cerebrospinal fluid drainage catheterization kit
Model / Ref / Catalog
826633, 82-6633
Primary DI / UDI-DI
10381780520436
510(k) Number
FDA product code
GWM
GMDN term
Ventricular cerebrospinal fluid drainage catheterization kit
Device class
Class II
Regulation number
882.1620
GUDID distribution status
In Commercial Distribution

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Other devices filed under Ventricular cerebrospinal fluid drainage catheterization kit.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)