TREADMILL MODEL 3060— 510(k) K792661

Name: FDA 510(k) clearance K792661
Creator: U.S. Food and Drug Administration
Published: 1980-02-19

Substantially Equivalent

Cambridge Instruments, Inc.

FDA 510(k) clearance K792661 for TREADMILL MODEL 3060, Substantially Equivalent on 1980-02-19. Applicant: Cambridge Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Cambridge Instruments, Inc.
Product code: Code IOL
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1979-12-26
Decision date: 1980-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOL

view all

K950376 — PARKER MODEL PM1995-09-06
K950377 — PARKER MODEL PE1995-09-06
K925839 — TRACKMASTER1993-06-24
K930261 — RTM REHABILITATION TREADMILL, MODEL #945-2001993-05-26
K904556 — MANSFIELD CARDIAC ASSIST MODEL 940(TM) IAB1991-12-18

More clearances from Cambridge Instruments, Inc.

view all

K811121 — CENTRAL STATION MONITORING SYSTEMS1981-06-30
K811062 — CAMPBRIDGE COMPUTRACE1981-05-29
K803229 — 4-CHANNEL ECG TELEMETRY MON. SYST. #30451981-01-13
K801224 — CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEM1980-06-26
K800566 — CAMBRIDGE VS-550 ELECTROCARDIOGRAPH1980-04-08

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