American Cystocope Makers, Inc.
American Cystocope Makers, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 29, 1983.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K832040 | STERILE FLUID PRODUCING UNIT #EP550 | Sep 29, 1983 |
| K812637 | ACMI BIPOLAR HEMOSTATIC SOURCE | Oct 26, 1981 |
| K811218 | ACMI ASPIRATOR KIT #8808 | Jul 1, 1981 |
| K803214 | ACMI BIPOLAR HEMOSTATIC ELECTRODE | Jan 15, 1981 |
| K791182 | ACMI RIGI-FLEX NEPHORSCOPE | Jul 30, 1979 |
| K770754 | DUODENOSCOPE, MOLEL TX-6 | Apr 28, 1977 |
| K760822 | MODEL TX-8 PANENDOSCOPE | Oct 21, 1976 |
| K760452 | COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92) | Aug 30, 1976 |
| K760451 | AIR WATER SOURCE (ACMI MODEL 710) | Aug 30, 1976 |