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MicroAire® 7505-040

by MicroAire Surgical Instruments LLC

MicroAire® 7505-040 is a Class II device made by MicroAire Surgical Instruments LLC, cleared under FDA 510(k) K032119 on 29 Oct 2003 and listed in FDA GUDID since 17 Sep 2022 (UDI-DI 00847399004840), 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) K032119

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 Number00847399004840 UDI-DI Date17 Sep 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK032119 Date29 Oct 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K032119 decided 29 Oct 2003 Active
  • FDA GUDID UDI-DI 00847399004840 listed 17 Sep 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K032119
  2. Listed FDA GUDID 00847399004840

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
MicroAire®
Generic name
Device sterilization/disinfection container, reusable
Model / reference
7505-040
Primary DI / UDI-DI
00847399004840
510(k) Number
FDA product code
KCT
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)