FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OP-CON SURGICAL INSTRUMENTS #4
K Number: K834173
·
Decision Dec 27, 1983
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
52
Review Days
36
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Basic Information
- Device Name
- OP-CON SURGICAL INSTRUMENTS #4
- K Number
- K834173
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.4530
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Imm Enterprises , Ltd.
- Date Received
- November 21, 1983
- Decision Date
- December 27, 1983
- Product Code
- LBX
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- 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 |
|---|---|---|---|
| LBX | Pelvimeter, Internal | FDA class 2 | Obstetrics/Gynecology |
Other Clearances by Imm Enterprises , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K840311 | CAT. 7-EAR, NOSE & THROAT DEVICES | May 9, 1984 | Substantially Equivalent |
| K841387 | WESTON RECTAL SNARE | May 9, 1984 | Substantially Equivalent |
| K841386 | KOLLMANN URETHRAL DILATOR | May 9, 1984 | Substantially Equivalent |
| K840304 | CATEGORY 17-MICROBIOLOGY DEVICES | May 1, 1984 | Substantially Equivalent |
| K840318 | CAT. 14-CLINICAL TOXIOLOGY DEVICES | Apr 23, 1984 | Substantially Equivalent |
| K840305 | CATEGORY 1 CIRCULATORY SYSTEM DEVICE | Apr 23, 1984 | Substantially Equivalent |
| K840312 | CAT. 8 DENTAL DEVICES | Apr 5, 1984 | Substantially Equivalent |
| K834171 | OP-CON SURG. INSTRUMENT #3 | Apr 4, 1984 | Substantially Equivalent |
| K834191 | JAKOBI SURGICAL INSTRUMENTS #3 17/18/19 | Mar 22, 1984 | Substantially Equivalent |
| K834192 | JAKOBI SURG. INSTRUMENTS #3 21/22/24 | Mar 22, 1984 | Substantially Equivalent |