FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELPHA 500
K Number: K823581
·
Decision Mar 24, 1983
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
5
Review Days
108
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Basic Information
- Device Name
- ELPHA 500
- K Number
- K823581
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Prothia USA, Inc.
- Date Received
- December 6, 1982
- Decision Date
- March 24, 1983
- Product Code
- GCJ
- Advisory Committee
- Gastroenterology, Urology
- 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 |
|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | FDA class 2 | Gastroenterology, Urology |
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