TREADMILL, DIAGNOSTIC— 510(k) K760509

Substantially Equivalent

Medcraft Corp.

FDA 510(k) clearance K760509 for TREADMILL, DIAGNOSTIC, Substantially Equivalent on 1976-08-30. Applicant: Medcraft Corp.. Device class: 1.

Clearance details

Applicant: Medcraft Corp.
Product code: Code IOL
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1976-08-24
Decision date: 1976-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOL

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 Medcraft Corp.

K860467 — ELECTROSHOCK UNIT NEUROLOGY MODEL B-251986-11-10
K791795 — COMP-ACT IV1979-09-27
K760508 — ACCUTAPE 241976-08-30
K760510 — MONITORING SYSTEM, REHABILITATION1976-08-30

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