FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
OPHTHALMIC KNIFE
K Number: K922378
·
Decision Dec 10, 1992
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
53
Applicant Total
1
Review Days
204
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- OPHTHALMIC KNIFE
- K Number
- K922378
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4350
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Microptics Development Laboratory
- Date Received
- May 20, 1992
- Decision Date
- December 10, 1992
- Product Code
- HNN
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HNN | Knife, Ophthalmic | FDA class 1 | Ophthalmic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HNN), ordered by most recent decision date.
CLEARCUT S SAFETY KNIFE
FDA 510(k)
FDA Class 1
·Ophthalmic
RETRACTIVE INCISION MICROMETER (RIM) GUAGE
FDA 510(k)
FDA Class 1
·Ophthalmic
MVR/STILETTO BLADE 20GA. - P/N 1900
FDA 510(k)
FDA Class 1
·Ophthalmic
PRISMA DISPOSABLE MVR/STILETTO BLADE
FDA 510(k)
FDA Class 1
·Ophthalmic
OPHTHALMIC TIP & BLADE SCALPELS
FDA 510(k)
FDA Class 1
·Ophthalmic
OPHTHALMIC DISPOSABLE BLADES
FDA 510(k)
FDA Class 1
·Ophthalmic