Home / 510(k) Clearances / K834555

510(k) K834555

BEAR VENTI--VOICE by Bear Medical Systems, Inc. — Product Code ESE

K834555 is an FDA 510(k) premarket notification submitted by Bear Medical Systems, Inc. for the device "BEAR VENTI--VOICE". The FDA issued a decision of Substantially Equivalent on January 24, 1984. The device falls under product code ESE (Larynx, Artificial (Battery-Powered)), a Class I device regulated under 21 CFR 874.3375. Bear Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1984
Date Received
December 27, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Larynx, Artificial (Battery-Powered)
Device Class
Class I
Regulation Number
874.3375
Review Panel
EN
Submission Type

Other clearances by Bear Medical Systems, Inc.

  • K992788 — BEAR CUB 750 PSV (September 16, 1999)
  • K983981 — BEAR 1000, VEOLAR W LEONARDO GRAPHICS, BICORE CP-2000, BICORE CP-100, HI-LO JET (November 20, 1998)
  • K912619 — BEAR 7 VENTILATOR (June 11, 1992)
  • K900637 — BEAR CEM CONTROLLER (August 3, 1990)
  • K896315 — BEAR VH820 DISPOSABLE CHAMBER ASSEMBLY (January 22, 1990)
  • K893034 — VHS 820 HUMIDIFIER, MODIFICATION (July 14, 1989)
  • K890724 — MOFIFICATION BEAR NVM-1 NEONATAL VOLUME MONITOR (March 30, 1989)
  • K882764 — BEAR EVC-100 CONTROLLER (September 30, 1988)
  • K881335 — BEAR 3 VENTILATOR (August 4, 1988)
  • K872660 — BEAR NVM-1 (February 12, 1988)

Other clearances for product code ESE

  • K934483 — NU-VOIS BATTERY POWERED ARTIFICIAL LARYNX (March 16, 1994)
  • K931371 — DENRICK SPEECH AID (DR-1) (August 25, 1993)
  • K923648 — LECTRO-LARYNX (April 7, 1993)
  • K914816 — AMERICAN ARTIFICIAL LARYNX (February 12, 1993)
  • K901503 — ADDVOX BONE CONDUCTOR AMPLIFIER SPEAKER SYSTEM (June 28, 1990)
  • K860992 — VOX COMPANION (May 2, 1986)
  • K860993 — P.O. VOX (April 25, 1986)
  • K854158 — RESNICK EMITTER, ARTIFICIAL LARYNX (December 13, 1985)
  • K840892 — ELECTRO-PALATE (May 22, 1984)
  • K834522 — VENTI-VOICE NASAL CATHETER (January 17, 1984)

FDA data resources