Cooper Medical, SRL
La Garita Alajuela, CR
COOPER MEDICAL, SRL appears in FDA device records in La Garita Alajuela, CR. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Cooper Medical, SRL between 1982 and 1984. The busiest year on record is 1984, with 4. The most recent is 1984, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1984 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K840144 | YAG LASER 8000 GASTROINTESTINAL BLEE | FCG | Substantially Equivalent | |
| K833387 | ARGON LASER SURGICAL SYSTEM 770 | Substantially Equivalent | ||
| K833497 | COOPER MEDICAL MODEL 770 | LLF | Substantially Equivalent | |
| K832703 | ARGON LASER SYS-MODEL 5000 | HQE | Substantially Equivalent | |
| K820261 | MONITOR CO2 LASER SYSTEM | HHR | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3014295858 | 3014295858 | COOPER MEDICAL, SRL | Edificio N B49, 51 Ave 0, La Garita Alajuela 20113 CR | 2026 | and 1 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- FCGBiopsy Needle
- MFDCannula, Intrauterine Insemination
- MQFCatheter, Assisted Reproduction
- HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered
- MQKLabware, Assisted Reproduction
- LLFLaser, Neurosurgical, Argon
- HHRLaser, Surgical, Gynecologic
- MQLMedia, Reproductive
- MQHMicrotools, Assisted Reproduction (Pipettes)
- PUCMicrotools, Assisted Reproduction (Pipettes), Exempt
- MQENeedle, Assisted Reproduction
- HHWPessary, Vaginal
- POVSemen Analysis Device
- GDWStaple, Implantable
- QQSStapler, Skin
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