KT-1000 DEVICE— 510(k) K812806

Substantially Equivalent

Medmetric Corp.

FDA 510(k) clearance K812806 for KT-1000 DEVICE, Substantially Equivalent on 1981-11-10. Applicant: Medmetric Corp.. Device class: 1.

Clearance details

Applicant: Medmetric Corp.
Product code: Code LYH
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1981-10-06
Decision date: 1981-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LYH

K943197 — KT1000/S KNEE LIGAMENT ARTHROMETER1995-03-02
K942059 — KT2000 KNEE LIGAMENT ARTHROMETER1994-09-20
K881876 — DYNAMIC CRUCIATE TESTER1988-11-17
K834462 — GENUCOM1984-02-09

More clearances from Medmetric Corp.

K904823 — FLEXERCYCLE1991-01-30
K904898 — TORQUE FRAME QTF10001990-11-28
K854254 — TENSION-ISOMETER1985-11-15
K812713 — DRAWER TEST1981-11-05
K801572 — SURG-ASSIST1980-08-04

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