FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
K Number: K871110
·
Decision Aug 27, 1987
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
187
Applicant Total
140
Review Days
161
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Basic Information
- Device Name
- CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
- K Number
- K871110
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.3450
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Edward Weck, Inc.
- Date Received
- March 19, 1987
- Decision Date
- August 27, 1987
- Product Code
- DSY
- 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 |
|---|---|---|---|
| DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | FDA class 2 | Cardiovascular |
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Other Clearances by Edward Weck, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K915378 | WECK TROCAR | Jun 29, 1992 | Substantially Equivalent |
| K914690 | LM15(TM), CATALOG NUMBER - 523821 | Mar 23, 1992 | Substantially Equivalent |
| K911915 | HEMOCLIP II | Jan 9, 1992 | Substantially Equivalent |
| K914470 | PNEUMO-SEAL(TM) | Nov 29, 1991 | Substantially Equivalent |
| K911272 | ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705 | Jul 2, 1991 | Substantially Equivalent |
| K902108 | HEM-O-LOK(TM) | Aug 6, 1990 | Substantially Equivalent |
| K902232 | WECK ELECTROSURGICAL GENERATOR #174200 | Aug 2, 1990 | Substantially Equivalent |
| K897045 | BOWIE-DICK TEST CARD CATALOG NUMBER 008018 | Feb 15, 1990 | Substantially Equivalent |
| K851251 | AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200 | Jul 2, 1985 | Substantially Equivalent |
| K851258 | WECK LX TM SKIN STAPLER | Jun 7, 1985 | Substantially Equivalent |