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AirLife 4MSF8-13

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 Number00607411961120 UDI-DI Date22 Nov 2018ListedStatusListed 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  • Withdrawn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
AirLife
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / Ref / Catalog
4MSF8-13
Primary DI / UDI-DI
00607411961120
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

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Cleared under the same submission (K151421)

Show all (12)

Other devices from Salter Labs, LLC

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No