Skip to content

MicroAire® ASP-CAN-NT

by MicroAire Surgical Instruments LLC 2 variants

MicroAire® ASP-CAN-NT is a Class II device made by MicroAire Surgical Instruments LLC, listed under FDA premarket submission BK220674 and listed in FDA GUDID since 19 May 2022 (UDI-DI 00847399017352), 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) BK220674

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 Number00847399017352 UDI-DI Date19 May 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberBK220674 Date—StatusActive

Official records

Across registries

2 registries list this device

  • FDA premarket submission BK220674 Active
  • FDA GUDID UDI-DI 00847399017352 listed 19 May 2022 Listed

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  • Withdrawn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
Liposuction system
Model / reference
ASP-CAN-NT
Primary DI / UDI-DI
00847399017352
FDA product code
MUU
GMDN term
Liposuction system
Device class
Class II
Regulation number
878.5040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Liposuction system

Cleared under the same submission (BK220674)

Similar devices in this category

Other devices filed under Liposuction system.

Other devices from MicroAire Surgical Instruments LLC

See all devices from MicroAire Surgical Instruments LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)