Argosy Electronics
FDA 510(k) medical device clearances.
Top product codes for Argosy Electronics
Recent clearances by Argosy Electronics
- K974242 — ARGOSY PROGRAMMABLE ONQUE
- K971699 — ARGOSY DYNAMEQ
- K961729 — ARGOSY PROGRAMMABLE
- K954038 — K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENT
- K952450 — WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROL
- K952451 — CLASS D LINEAR WITH ACTIVE TONE CONTROL
- K952452 — OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL
- K952453 — INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROL
- K952454 — EXPANDER WITH ACTIVE TONE CONTROL
- K952455 — IMPROVED MANHATTAN II
- K944078 — PROGRAM 3-CH SER HEAR AIDS W/PROGRAM FIT SYST/PRO FIT
- K944077 — PROGRAM 3-CH SERIES HEAR AIDS W/DT-1 DESKTOP PROGRAM
- K940116 — COMPLETELY IN THE CANAL
- K934452 — HI BAND
- K934442 — LINEAR PLUS
- K934443 — 2:1 INPUT COMPRESSION
- K934444 — K-AMP
- K934446 — POWER MANHATTAN II
- K934447 — LINEAR PLUS-POWER
- K934448 — POWER 3-CHANNEL-CLOCK
- K934449 — 3-CHANNEL K-AMP
- K934450 — MANHATTAN 3-CHANNEL
- K934453 — 3-CHANNEL CLOCK
- K934454 — MANHATTAN II
Data sourced from openFDA. This site is unofficial and independent of the FDA.