THE BTE DYNAMIC LIFT— 510(k) K924414

Name: FDA 510(k) clearance K924414
Creator: U.S. Food and Drug Administration
Published: 1993-02-12

Substantially Equivalent

Baltimore Therapeutic Equipment Co.

FDA 510(k) clearance K924414 for THE BTE DYNAMIC LIFT, Substantially Equivalent on 1993-02-12. Applicant: Baltimore Therapeutic Equipment Co.. Device class: 2.

Clearance details

Applicant: Baltimore Therapeutic Equipment Co.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1992-08-31
Decision date: 1993-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hanover, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKK

view all

K123746 — AMES THERAPY DEVICE2013-05-24
K952090 — HUMAC SYSTEM1995-12-11
K951770 — BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP1995-11-16
K951916 — CC RIDER, MODEL ME1801995-10-04
K950095 — CYBEX 7701995-06-21

More clearances from Baltimore Therapeutic Equipment Co.

view all

K955105 — BTE CPM-101995-12-29
K955106 — BTE CPM-201995-12-29
K925225 — THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK1994-06-27
K933611 — THE BTE WS301994-06-20
K895881 — MOTIONSPECT1990-04-10

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