Argosy Electronics
Eden Prairie, MN, US
Argosy Electronics appears in FDA device records in Eden Prairie, MN. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Argosy Electronics between 1993 and 1998. The busiest year on record is 1993, with 11. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 11 |
| 1994 | 3 |
| 1995 | 7 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K974242 | ARGOSY PROGRAMMABLE ONQUE | ESD | Substantially Equivalent | |
| K971699 | ARGOSY DYNAMEQ | ESD | Substantially Equivalent | |
| K961729 | ARGOSY PROGRAMMABLE | ESD | Substantially Equivalent | |
| K954038 | K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENT | ESD | Substantially Equivalent | |
| K952452 | OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL | ESD | Substantially Equivalent | |
| K952451 | CLASS D LINEAR WITH ACTIVE TONE CONTROL | ESD | Substantially Equivalent | |
| K952450 | WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROL | ESD | Substantially Equivalent | |
| K952455 | IMPROVED MANHATTAN II | ESD | Substantially Equivalent | |
| K952454 | EXPANDER WITH ACTIVE TONE CONTROL | ESD | Substantially Equivalent | |
| K952453 | INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROL | ESD | Substantially Equivalent | |
| K944078 | PROGRAM 3-CH SER HEAR AIDS W/PROGRAM FIT SYST/PRO FIT | ESD | Substantially Equivalent | |
| K944077 | PROGRAM 3-CH SERIES HEAR AIDS W/DT-1 DESKTOP PROGRAM | ESD | Substantially Equivalent | |
| K940116 | COMPLETELY IN THE CANAL | ESD | Substantially Equivalent | |
| K934452 | HI BAND | ESD | Substantially Equivalent | |
| K934454 | MANHATTAN II | ESD | Substantially Equivalent | |
| K934453 | 3-CHANNEL CLOCK | ESD | Substantially Equivalent | |
| K934450 | MANHATTAN 3-CHANNEL | ESD | Substantially Equivalent | |
| K934449 | 3-CHANNEL K-AMP | ESD | Substantially Equivalent | |
| K934448 | POWER 3-CHANNEL-CLOCK | ESD | Substantially Equivalent | |
| K934447 | LINEAR PLUS-POWER | ESD | Substantially Equivalent | |
| K934446 | POWER MANHATTAN II | ESD | Substantially Equivalent | |
| K934444 | K-AMP | ESD | Substantially Equivalent | |
| K934443 | 2:1 INPUT COMPRESSION | ESD | Substantially Equivalent | |
| K934442 | LINEAR PLUS | ESD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain