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Salter Labs® Nasal Cannula 13347

by Salter Labs, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00607411919213 UDI-DI Date10 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Salter Labs® Nasal Cannula
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / Reference
13347
Primary DI / UDI-DI
00607411919213
510(k) Number
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

Related devices

Cleared under the same submission (K151421)

Show all (12)

Other devices from Salter Labs, LLC

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Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No