Skip to content

Thermometer, Mercury/Clinical

by Perlink USA, Inc. 510(k)

Active United States

510(k) K901790

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK901790 Date11 Jul 1990ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • 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
FLK
Device Class
Class II
Regulation
21 CFR Part 880.2920
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Other devices from Perlink USA, Inc.