Acrymed, Inc.
Portland, OR, US
Acrymed, Inc. appears in FDA device records in Portland, OR. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Acrymed, Inc. between 1994 and 2009. The busiest year on record is 2000, with 3. The most recent is 2009, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 1 |
| 1996 | 1 |
| 1997 | 1 |
| 1999 | 1 |
| 2000 | 3 |
| 2001 | 2 |
| 2006 | 1 |
| 2007 | 1 |
| 2008 | 1 |
| 2009 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K091354 | ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSING | FRO | Substantially Equivalent | |
| K083103 | ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #B | FRO | Substantially Equivalent | |
| K082459 | ACRYDERM ABSORBENT OXYGEN DRESSING | FRO | Substantially Equivalent | |
| K070333 | ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL | FRO | Substantially Equivalent | |
| K061232 | ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006 | FRO | Substantially Equivalent | |
| K011994 | ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 | MGQ | Substantially Equivalent | |
| K012116 | ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING | FRO | Substantially Equivalent | |
| K002909 | ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103 | FRO | Substantially Equivalent | |
| K002599 | MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045 | FRO | Substantially Equivalent | |
| K991818 | ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045 | FRO | Substantially Equivalent | |
| K992032 | ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033 | KMF | Substantially Equivalent | |
| K970693 | ACRYDERM GEL WOUND DRESSING | MGQ | Substantially Equivalent for Some Indications | |
| K962851 | ACRYNOODLES ABSORBENT WOUND DRESSING | MGQ | Substantially Equivalent | |
| K943781 | ACRYDERM ADVANCED WOUND DRESSING | KMF | Substantially Equivalent for Some Indications |
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