CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT— 510(k) K902625

Name: FDA 510(k) clearance K902625
Creator: U.S. Food and Drug Administration
Published: 1990-10-26

Substantially Equivalent

Liaoning-Usa Corp.

FDA 510(k) clearance K902625 for CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT, Substantially Equivalent on 1990-10-26. Applicant: Liaoning-Usa Corp.. Device class: 2.

Clearance details

Applicant: Liaoning-Usa Corp.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1990-06-14
Decision date: 1990-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pasadena, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FLK

view all

K960185 — AMSINO CLINICAL THERMOMETER1996-03-28
K960224 — GERATHERM MERCUIRY FREE CLINICAL THERMOMETER1996-03-25
K953465 — KENTEMP1995-12-15
K942483 — CLINICAL GLASS THERMOMETER1995-03-28
K941673 — MEDIAID UNIVERSAL THERMOMETER1994-08-25

More clearances from Liaoning-Usa Corp.

view all

K911921 — DISPOSABLE ISOLATION GOWN1991-05-13
K905487 — VARIOUS TYPES OF STETHOSCOPES1991-04-09
K910623 — GAUZE SPONGES ABSORBENT GAUZE ROLLS1991-04-01
K892781 — ANTELOPE BRAND PATIENT EXAMINATION GLOVES1989-09-21
K892774 — PATIENT EXAMINATION GLOVES1989-09-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.