FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MEDGENERAL SINGLE-USE BULLDOG
K Number: K782006
·
Decision Dec 15, 1978
Classifications
1
FEI Numbers
270
Registration Numbers
270
Same Product Code
31
Applicant Total
12
Review Days
14
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Basic Information
- Device Name
- MEDGENERAL SINGLE-USE BULLDOG
- K Number
- K782006
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Med General
- Date Received
- December 1, 1978
- Decision Date
- December 15, 1978
- Product Code
- GDJ
- 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 |
|---|---|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GDJ), ordered by most recent decision date.
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Other Clearances by Med General
| K Number | Device Name | ||
|---|---|---|---|
| K791097 | CEPTORTRODE WITH CEPTOR HESIVE | Aug 3, 1979 | Substantially Equivalent |
| K791098 | SINGLE-USE MINI-BULLDOG | Jun 22, 1979 | Substantially Equivalent |
| K790763 | MAXI-VAC TM | Apr 23, 1979 | Substantially Equivalent |
| K790269 | CEPTOR HESIVE | Feb 26, 1979 | Substantially Equivalent |
| K781239 | MYO-STIM | Nov 3, 1978 | Substantially Equivalent |
| K780632 | MAXICEPTOR | Aug 14, 1978 | Substantially Equivalent |
| K780698 | STIMULATORS, NERVE, ELECTRICAL | May 12, 1978 | Substantially Equivalent |
| K780117 | CARDIOMETER | Feb 3, 1978 | Substantially Equivalent |
| K771701 | VESSEL-CLUDE | Dec 13, 1977 | Substantially Equivalent |
| K771702 | VESSEL-STABILIZER | Dec 13, 1977 | Substantially Equivalent |