THERMOMETER SHEATHES, STERILE (GLASS)— 510(k) K870285

Name: FDA 510(k) clearance K870285
Creator: U.S. Food and Drug Administration
Published: 1987-02-12

Substantially Equivalent

The Medical Group, Inc.

FDA 510(k) clearance K870285 for THERMOMETER SHEATHES, STERILE (GLASS), Substantially Equivalent on 1987-02-12. Applicant: The Medical Group, Inc.. Device class: 2.

Clearance details

Applicant: The Medical Group, Inc.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1987-01-27
Decision date: 1987-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Reno, NV, 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 The Medical Group, Inc.

view all

K911246 — THE MEDISCUS PEDCARE MANAGEMENT SYSTEM-MODEL 21991-06-06
K901295 — PULMONAIR 40 PATIENT MANAGEMENT SYSTEM1990-03-30
K881843 — PEDIATRIC HOSPITAL BED1988-10-26
K881844 — MAGNUM 800(TM) MANAGEMENT SYSTEM1988-07-14
K870282 — 4 X 4 SPONGES, NON-STERILE1987-02-24

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