FDA 510(k)
FDA class 3
Substantially Equivalent
🇺🇸 United States
ISOLATION SLEEVE, MODEL 347-01
K Number: K790099
·
Decision Jan 24, 1979
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
211
Review Days
8
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- ISOLATION SLEEVE, MODEL 347-01
- K Number
- K790099
- Device Class
- FDA class 3
- Clearance Type
- Traditional
- Regulation Number
- 870.3610
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Intermedics, Inc.
- Date Received
- January 16, 1979
- Decision Date
- January 24, 1979
- Product Code
- DXY
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DXY | Implantable Pacemaker Pulse-Generator | FDA class 3 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DXY), ordered by most recent decision date.
PIKOS 01, PIKOS E01, PIKOS 01-B, PIKOS E01-B, PIKOS 01-A, PIKOS E01-A
FDA 510(k)
FDA Class 3
·Cardiovascular
OPUS S MODEL 4121 AND 4124 PACEMAKERS
FDA 510(k)
FDA Class 3
·Cardiovascular
PIKOS LP 01, PIKOS LP E01
FDA 510(k)
FDA Class 3
·Cardiovascular
ALTERNATE STERLIZATION PROCESS & MODIFIED DF-1 LEAD CONNECTOR (MODIFICATION)
FDA 510(k)
FDA Class 3
·Cardiovascular
MINIX 834M & MINIX ST 8331M PULSE GENERATORS (MODIFICATION)
FDA 510(k)
FDA Class 3
·Cardiovascular
MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS
FDA 510(k)
FDA Class 3
·Cardiovascular
Other Clearances by Intermedics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K954610 | MODEL 430-07 ENDOCARDIAL PACING LEAD | Dec 16, 1996 | Substantially Equivalent - Subject to Tracking & PMS |
| K955122 | INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD | Nov 4, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K962174 | BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07) | Aug 21, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K955550 | CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD | Jun 19, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K960281 | IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY | Jun 18, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K954719 | INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD | Feb 27, 1996 | Substantially Equivalent - Subject to Tracking Reg. |
| K933278 | INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04 | Mar 15, 1995 | Substantially Equivalent |
| K922042 | CARDIFIX ENDOCARDIAL PACING LEAD | Apr 29, 1993 | Unknown |
| K922972 | MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD | Jan 22, 1993 | Unknown |
| K920530 | INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG | Mar 17, 1992 | Substantially Equivalent |