FDA 510(k)
Unknown
🇺🇸 United States
QUINTREX 0515 PROGRAMMABLE PULSE GEN.
K Number: K802223
·
Decision Sep 12, 1980
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
8
Review Days
—
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Basic Information
- Device Name
- QUINTREX 0515 PROGRAMMABLE PULSE GEN.
- K Number
- K802223
- Clearance Type
- Traditional
- Decision
- Unknown
- Applicant
- Medcor, Inc.
- Date Received
- September 12, 1980
- Decision Date
- September 12, 1980
- Advisory Committee
- Unknown
- Review Advisory Committee
- CV
- Third Party
- N
Other Clearances by Medcor, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K792609 | LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN. | Nov 19, 1980 | Substantially Equivalent |
| K802224 | QUINTREX 0516 PROG. PULSE GENERATOR SYS | Sep 12, 1980 | Unknown |
| K791678 | LITHICRON II 0403 IMPLANTABLE PACEMAKER | Sep 7, 1979 | Substantially Equivalent |
| K791095 | LITHICRON MODEL 0401, PACEMAKER | Aug 10, 1979 | Substantially Equivalent |
| K780430 | LITHICRON F PROGRAMMABLE PULSE GEN | Dec 22, 1978 | Substantially Equivalent |
| K771538 | LITHICRON MODEL 3-70C-B PULSE GENERATOR | Aug 22, 1977 | Substantially Equivalent |
| K770507 | PULSE GENERATOR, LITKICRON MODEL 3-70H | Apr 7, 1977 | Substantially Equivalent |