Microsurge, Inc.
North Attleboro, MA, US
Microsurge, Inc. appears in FDA device records in North Attleboro, MA. FDA records list 15 510(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
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Microsurge, Inc. between 1991 and 1996. The busiest year on record is 1995, with 5. The most recent is 1996, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 2 |
| 1993 | 4 |
| 1994 | 1 |
| 1995 | 5 |
| 1996 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K964109 | MICROSURGE LAPAROSCOPIC PERMACLIP CARTRIDGE WITH IMPLANTABLE CLIP | FZP | Substantially Equivalent | |
| K960554 | DETACHATIP THORACOSCOPIC SCISSORS | GEI | Substantially Equivalent | |
| K955408 | MICROSURGE THORACOSCOPIC INSTRUMENTS | GCJ | Substantially Equivalent | |
| K954641 | ENDO-LEADER | OCW | Substantially Equivalent | |
| K954072 | MICROSURGE PUNCTURE CLOSE DEVICE | GCJ | Substantially Equivalent | |
| K954520 | MICROSURGE VERESS NEEDLE | HET | Substantially Equivalent | |
| K953121 | MICROSURGE THORACOSCOPIC ACCESS SYSTEM | GCJ | Substantially Equivalent | |
| K951230 | MICROSURGE BIPOLAR GRASPERS | GEI | Substantially Equivalent | |
| K933750 | MICROSURGE REUSABLE FRONT END GRASP DEVICES, MODIF | GCJ | Substantially Equivalent | |
| K930355 | MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS | GEI | Substantially Equivalent | |
| K925830 | MICROSURGE SUCTION/IRRIGATION SYSTEM | GEI | Substantially Equivalent | |
| K924283 | MICROSURGE DETACHA-TIP SURGICAL INSTRUMENTS | GEI | Substantially Equivalent | |
| K922802 | MICROSURGE FRONT-END GRASPING DEVICES | GEI | Substantially Equivalent | |
| K914175 | MICROSURGE LASER FIBER WITH SMA CONNECTOR | GEX | Substantially Equivalent | |
| K912332 | MICROSURGE LASER FIBER HOLDER | GEX | 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