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Apk A1202-SA125PU

by Apk Technology

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06946725553169 UDI-DI Date13 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Apk
Generic Name
Pulse oximeter probe, single-use
Model / Reference
A1202-SA125PU
Primary DI / UDI-DI
06946725553169
510(k) Number
FDA Product Code
DQA
GMDN Term
Pulse oximeter probe, single-use
Device Class
Class II
Regulation Number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K082846)

Show all (12)

Other devices from Apk Technology

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Properties

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

Other properties (10)

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