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Gas Sampling Lines 0512

by Salter Labs, LLC

Gas Sampling Lines 0512 is a Class II device made by Salter Labs, LLC, cleared under FDA 510(k) K930957 on 2 Jul 1993 and listed in FDA GUDID since 31 Oct 2023 (UDI-DI 10889483224229), 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) K930957

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 Number10889483224229 UDI-DI Date31 Oct 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESK from GUDID Substantially Equivalent — Kit · Traditional NumberK930957 Date2 Jul 1993DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K930957 decided 2 Jul 1993 Active
  • FDA GUDID UDI-DI 10889483224229 listed 31 Oct 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K930957
  2. Listed FDA GUDID 10889483224229

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Gas Sampling Lines
Generic name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / reference
0512
Primary DI / UDI-DI
10889483224229
FDA product code
CCK
GMDN term
Nasal oxygen cannula, carbon-dioxide-sampling
Device class
Class II
Regulation number
868.1400
GUDID distribution status
In Commercial Distribution

Other devices from Salter Labs, LLC

See all devices from Salter Labs, LLC →

Properties

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