INOX THERMOMETER JAR— 510(k) K852301

Substantially Equivalent

Broadwest Corp.

FDA 510(k) clearance K852301 for INOX THERMOMETER JAR, Substantially Equivalent on 1985-07-01. Applicant: Broadwest Corp.. Device class: 2.

Clearance details

Applicant: Broadwest Corp.
Product code: Code FLK
Device class: Class 2
Regulation: 21 CFR 880.2920
Advisory panel: General Hospital
Date received: 1985-05-29
Decision date: 1985-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FLK

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 Broadwest Corp.

K864499 — PODOSCOPE1987-02-04
K864569 — PODODIGITAL1987-02-04
K852302 — INOX IORCEPS JAR1985-07-02
K852300 — INOX IV STAND1985-06-20
K851307 — INOX DRY HEAT STERILIZER1985-05-09

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