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Mms T3 Uptake

by Micromedic Systems 510(k)

Active United States

510(k) K861262

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK861262 Date23 May 1986ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 10 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KHQ
Device Class
Class II
Regulation
21 CFR Part 862.1715
Advisory Committee
Clinical Chemistry
FDA Decision
SESE Substantially Equivalent

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