FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
A.C.L. GUIDE KIT
K Number: K862564
·
Decision Aug 18, 1986
Classifications
1
FEI Numbers
526
Registration Numbers
526
Same Product Code
18
Applicant Total
55
Review Days
46
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Basic Information
- Device Name
- A.C.L. GUIDE KIT
- K Number
- K862564
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Aspen Laboratories, Inc.
- Date Received
- July 3, 1986
- Decision Date
- August 18, 1986
- Product Code
- FZX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FZX | Guide, Surgical, Instrument | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
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Other Clearances by Aspen Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K981220 | SYSTEM 7500 ABC ELECTROSURGICAL UNIT | Apr 21, 1998 | Substantially Equivalent |
| K963088 | SHEATH, ELECTROSURGICAL PENCIL | Sep 13, 1996 | Substantially Equivalent |
| K955834 | SYSTEM 6500 ABC ELECTROSURGICAL UNIT | Jul 11, 1996 | Substantially Equivalent |
| K960296 | 4000 ETM | Feb 20, 1996 | Substantially Equivalent |
| K953081 | BEAMER PLUS | Oct 30, 1995 | Substantially Equivalent |
| K953007 | EXCALIBUR PLUS ELECTROSURGICAL UNIT | Aug 21, 1995 | Substantially Equivalent |
| K946104 | SMOKIEVAC ELECTROSURGICAL PENCIL | Apr 3, 1995 | Substantially Equivalent |
| K944012 | ELECTROSURGICAL FLEXIBLE ELECTRODE IN-LINE SUCTION COAGULATOR | Dec 21, 1994 | Substantially Equivalent |
| K924960 | EXCALIBUR ELECTROSURGICAL UNIT | Apr 16, 1993 | Substantially Equivalent |
| K913213 | SINGLE USE LEE ELECTRODE | Feb 13, 1992 | Substantially Equivalent |