Home / 510(k) Clearances / K940683

510(k) K940683

WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA by Wahl Clipper Corp. — Product Code ISA

K940683 is an FDA 510(k) premarket notification submitted by Wahl Clipper Corp. for the device "WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISA". The FDA issued a decision of SN on June 9, 1994. The device falls under product code ISA (Massager, Therapeutic, Electric), a Class I device regulated under 21 CFR 890.5660. Wahl Clipper Corp. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
June 9, 1994
Date Received
February 10, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Massager, Therapeutic, Electric
Device Class
Class I
Regulation Number
890.5660
Review Panel
PM
Submission Type

Other clearances by Wahl Clipper Corp.

  • K944909 — WAHL FRESH FACE (May 8, 1995)
  • K950701 — WAHL SPORTS RELIEF HOT/COLD MASSAGER ROLLER (March 24, 1995)
  • K946162 — 3M(TM) SURGICAL SLIPPER, 9660 SERIES (January 24, 1995)
  • K944024 — STIMU-TAP (December 8, 1994)
  • K941594 — WAHL DOUBLE COMFORT MASSAGER (June 9, 1994)
  • K941412 — WAHL COMPACT COMFORT MASSAGER (June 9, 1994)
  • K940837 — WAHL(R) FOOT COMFORT MASSAGER (June 9, 1994)

Other clearances for product code ISA

  • K243488 — VMAT PRO (February 6, 2025)
  • K240358 — ShockPhysio Mobile (model SW3200 Basic) (June 5, 2024)
  • K221865 — BTL-094 (April 14, 2023)
  • K210166 — Omnispec ED1000 (January 27, 2023)
  • K213120 — OW100S (model OW100S-US) (October 12, 2022)
  • K220538 — DolorClast Radial (July 11, 2022)
  • K210451 — OrthoGold 100 (May 5, 2021)
  • K182682 — OrthoGold 100 (December 21, 2018)
  • K173692 — D-Actor 200 Vibration Massage System (April 13, 2018)
  • K053225 — CELLU M6 KEYMODULE I (November 6, 2006)

FDA data resources