REMOVABLE BATTERY POWER SYSTEM— 510(k) K885106

Name: FDA 510(k) clearance K885106
Creator: U.S. Food and Drug Administration
Published: 1988-12-27

Substantially Equivalent

Rolcontrol Products, Co., Inc.

FDA 510(k) clearance K885106 for REMOVABLE BATTERY POWER SYSTEM, Substantially Equivalent on 1988-12-27. Applicant: Rolcontrol Products, Co., Inc.. Device class: 1.

Clearance details

Applicant: Rolcontrol Products, Co., Inc.
Product code: Code KNN
Device class: Class 1
Regulation: 21 CFR 890.3920
Advisory panel: Physical Medicine
Date received: 1988-12-12
Decision date: 1988-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNN

view all

K211919 — KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat2022-03-04
K942308 — DYNASTY GC 12400 (GELL/CELL)1994-11-07
K942309 — DYNASTY U1-31 (GELL/CELL)1994-11-07
K942310 — DYNASTY GC 12550 (GELL/CELL)1994-11-07
K942311 — DYNASTY U1-33 AGM1994-11-07

More clearances from Rolcontrol Products, Co., Inc.

view all

K885103 — 1600 LIGHT TOUCH CONTROL1988-12-27
K885104 — LAYDOWN ARM SUPPORT MECHANISM1988-12-27
K885105 — SLIDING ARM SUPPORT1988-12-27
K883671 — 805 POWER CHAIR CONVERSION SYSTEM1988-09-13
K883672 — PARALYZED VETERANS OF AMERICA POWER RECLINER1988-09-13

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