FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BOUGIE, FILIFORM, JACKSON
K Number: K770959
·
Decision Jun 14, 1977
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
0
Applicant Total
41
Review Days
18
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Basic Information
- Device Name
- BOUGIE, FILIFORM, JACKSON
- K Number
- K770959
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.4175
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- V. Mueller O.V. Baxter Healthcare Corp.
- Date Received
- May 27, 1977
- Decision Date
- June 14, 1977
- Product Code
- KBI
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| KBI | Bougie, Eustachian | FDA class 1 | Ear, Nose, Throat |
Other Clearances by V. Mueller O.V. Baxter Healthcare Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K803292 | FIELD SUCTION DISSECTOR | Jan 29, 1981 | Substantially Equivalent |
| K792383 | KELMAN DIPSTICK | Dec 11, 1979 | Substantially Equivalent |
| K771197 | NORTON ENDOTRACHEAL | Aug 16, 1977 | Substantially Equivalent |
| K771302 | PFISTER-SCHWARTZ STONE RETRIEVER | Aug 2, 1977 | Substantially Equivalent |
| K770280 | CORD, ELECTROSURGICAL-STERILE & DISPOS. | Apr 15, 1977 | Substantially Equivalent |
| K760851 | CONVERSE ALTAR RETRACTOR | Mar 10, 1977 | Substantially Equivalent |
| K761242 | TEFLON COATED RESECTOSCOPE SHEATH | Dec 16, 1976 | Substantially Equivalent |
| K760273 | LITHOTRITE | Dec 6, 1976 | Substantially Equivalent |
| K760172 | OBTURATOR, VISUAL | Dec 2, 1976 | Substantially Equivalent |
| K760180 | FORCEPS, GRASPING | Dec 2, 1976 | Substantially Equivalent |