FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
K Number: K892856
·
Decision Nov 8, 1989
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
41
Applicant Total
12
Review Days
204
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Basic Information
- Device Name
- NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
- K Number
- K892856
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.4200
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Acacia Laboratories, Inc.
- Date Received
- April 18, 1989
- Decision Date
- November 8, 1989
- Product Code
- KRI
- 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 |
|---|---|---|---|
| KRI | Accessory Equipment, Cardiopulmonary Bypass | FDA class 1 | Cardiovascular |
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Other Clearances by Acacia Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K952419 | STERIGAUZE GEL DRESSING | Jul 26, 1995 | Substantially Equivalent |
| K952420 | STERIGAUZE WET DRESSING | Jul 12, 1995 | Substantially Equivalent |
| K951861 | STERICARE WOUND CARE GEL | Jul 11, 1995 | Substantially Equivalent |
| K952414 | PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER | Jun 23, 1995 | Substantially Equivalent |
| K951914 | HYDRACARE ABSORBENT WOUND DRESSING | May 15, 1995 | Substantially Equivalent for Some Indications |
| K950344 | HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER | Mar 24, 1995 | Unknown |
| K913408 | STERILE PLASTIC DRAPE | Mar 12, 1992 | Substantially Equivalent |
| K901761 | STERILE SUCTION TUBING SET | May 7, 1990 | Substantially Equivalent |
| K892804 | NEWCHILL(TM) CARDIAC INSULATOR | Jul 14, 1989 | Substantially Equivalent |
| K884055 | SURGI-TAG(TM) STERILE LABEL SETS | Oct 13, 1988 | Substantially Equivalent |