FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CAMSYS 6300
K Number: K920574
·
Decision Feb 17, 1993
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
6
Applicant Total
12
Review Days
376
Basic Information
- Device Name
- CAMSYS 6300
- K Number
- K920574
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1620
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- F.M. WIEST USA, INC.
- Date Received
- February 7, 1992
- Decision Date
- February 17, 1993
- Product Code
- EXQ
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| EXQ | Cystometer, Electrical Recording | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by F.M. WIEST USA, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K921871 | HYSTEROMAT(TM) 3700 | Dec 15, 1994 | Substantially Equivalent |
| K920575 | MERKUR 4000 | Jul 23, 1992 | Substantially Equivalent |
| K915751 | URETEROMAT 4400 | Apr 24, 1992 | Substantially Equivalent |
| K911844 | HYSTEROFLATOR 1500 | Nov 21, 1991 | Substantially Equivalent |
| K912071 | SPACE(TM) 7500 | Jul 9, 1991 | Substantially Equivalent |
| K910883 | LAPAROFLATOR ELECTRONIC 3509 | Mar 29, 1991 | Substantially Equivalent |
| K875137 | LAPAROFLATOR 3000, STANDARD AND ELECTRONIC | Mar 2, 1988 | Substantially Equivalent |
| K871181 | ARTHROCOMBI 5003 | Sep 29, 1987 | Substantially Equivalent |
| K871180 | ARTHRO AUTOMAT 5002 | Sep 29, 1987 | Substantially Equivalent |
| K865066 | ARTHROFLATOR | Apr 20, 1987 | Substantially Equivalent |