FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STERILE PLASTIC DRAPE
K Number: K913408
·
Decision Mar 12, 1992
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
12
Review Days
226
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Basic Information
- Device Name
- STERILE PLASTIC DRAPE
- K Number
- K913408
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4370
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Acacia Laboratories, Inc.
- Date Received
- July 30, 1991
- Decision Date
- March 12, 1992
- Product Code
- KKX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KKX | Drape, Surgical, Antimicrobial | FDA class 2 | General, Plastic Surgery |
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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 |
| K901761 | STERILE SUCTION TUBING SET | May 7, 1990 | Substantially Equivalent |
| K892856 | NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS | Nov 8, 1989 | Substantially Equivalent |
| K892804 | NEWCHILL(TM) CARDIAC INSULATOR | Jul 14, 1989 | Substantially Equivalent |
| K884055 | SURGI-TAG(TM) STERILE LABEL SETS | Oct 13, 1988 | Substantially Equivalent |