FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BENCHMARK III
K Number: K922447
·
Decision Aug 5, 1992
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
193
Applicant Total
55
Review Days
75
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Basic Information
- Device Name
- BENCHMARK III
- K Number
- K922447
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.3060
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- J.F. Jelenko & Co., Inc.
- Date Received
- May 22, 1992
- Decision Date
- August 5, 1992
- Product Code
- EJS
- Advisory Committee
- Dental
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| EJS | Alloy, Other Noble Metal | FDA class 2 | Dental |
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Other Clearances by J.F. Jelenko & Co., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K012303 | JEL-20 | Aug 22, 2001 | Substantially Equivalent |
| K002993 | HERACERAM | Nov 16, 2000 | Substantially Equivalent |
| K002645 | JEL BIOS PURE | Oct 19, 2000 | Substantially Equivalent |
| K002222 | RD-2104 | Aug 31, 2000 | Substantially Equivalent |
| K001360 | SIGNUM | Jun 20, 2000 | Substantially Equivalent |
| K001260 | ALLROUND 55 LF | May 17, 2000 | Substantially Equivalent |
| K001196 | JEL BIOS 90 (CODE NAME RD-2401) | May 11, 2000 | Substantially Equivalent |
| K000532 | JEL 15 | Apr 6, 2000 | Substantially Equivalent |
| K993136 | JEL BIOS 10 (CODE NAME RD-1801) | Oct 21, 1999 | Substantially Equivalent |
| K993152 | JEL BIOS 18 (CODE NAME RD- 1214) | Oct 21, 1999 | Substantially Equivalent |