Neuromed, Inc.
Ft. Lauderdale, FL, US
Neuromed, Inc. appears in FDA device records in Ft. Lauderdale, FL. 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 Neuromed, Inc. between 1985 and 1996. The busiest year on record is 1985, with 3. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 3 |
| 1986 | 3 |
| 1990 | 1 |
| 1991 | 3 |
| 1993 | 1 |
| 1994 | 3 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960728 | ONE STEP CONNECT LEADS (QUATTRODE, OCTRODE, CERVITRODE) | GZB | Substantially Equivalent | |
| K930536 | NEUROMED OCTRODE MODEL MNR-88A-B-C NEUROSTIM REC | GZB | Substantially Equivalent | |
| K930498 | NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN | GZB | Substantially Equivalent | |
| K930242 | INTRODE INT-8 | GZB | Substantially Equivalent | |
| K921319 | NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30 | GZB | Substantially Equivalent | |
| K905596 | NEUROMED OCTRODE MODEL MNR-88B/88C NEUROSTIM SYST | GZB | Substantially Equivalent | |
| K905255 | NEUROMED MODEL 1992 LS LAMITRODE LEAD | GZB | Substantially Equivalent | |
| K903814 | NEUROMED TS8 TEST STIMULATOR | GZB | Substantially Equivalent | |
| K901499 | NEUROMED OCTRODE MODEL MNR-88 W/98 ADAPTER NEURO. | GZB | Substantially Equivalent | |
| K862915 | MULTISTIM(4-CHANNEL), MULTISTIM-OCTRODE(8 CHANNEL) | GZB | Substantially Equivalent | |
| K860185 | UNISTIM UNT-1M NEUROSTIMULATOR TRANSMITTER | GZB | Substantially Equivalent | |
| K860158 | 8-CHANNEL MULTIPROG IMPLANT SPINAL CORD STIMULATOR | GZB | Substantially Equivalent | |
| K853643 | MULTISTIM LAMINECTOMY ELECTRODE | GZB | Substantially Equivalent | |
| K852326 | UNISTIM UNT-1 | GZB | Substantially Equivalent | |
| K852920 | QUADRA CATH ELECT(3MM SIZES) 1990J, JF, JP + JPF | GZB | 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