Conceptus, Inc.
San Carlos, CA, US
Conceptus, Inc. appears in FDA device records in San Carlos, CA. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Conceptus, Inc. between 1994 and 1998. The busiest year on record is 1995, with 3. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 2 |
| 1995 | 3 |
| 1996 | 1 |
| 1997 | 2 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K974028 | STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBING | MKO | Substantially Equivalent | |
| K972210 | RESECTOSCOPE SAFETY SHEATH | HIH | Substantially Equivalent | |
| K962587 | CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM | MKO | Substantially Equivalent | |
| K954164 | HYSTEROSCOPE | HIH | Substantially Equivalent | |
| K953314 | CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM | MOV | Substantially Equivalent | |
| K932387 | CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL | HET | Substantially Equivalent | |
| K932993 | INTRAUTERINE CATHETER AND INTRODUCER | MFD | Substantially Equivalent | |
| K933981 | CERVICAL CATHETER | LKF | Substantially Equivalent | |
| K933723 | CONCEPTUS UTERINE CATHETER | LKF | 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