FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DUNRICH TABLES
K Number: K800756
·
Decision Apr 16, 1980
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
31
Applicant Total
1
Review Days
12
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
- DUNRICH TABLES
- K Number
- K800756
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.5300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- Dunrich, Inc.
- Date Received
- April 4, 1980
- Decision Date
- April 16, 1980
- Product Code
- ETF
- 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 |
|---|---|---|---|
| ETF | Unit, Examining/Treatment, Ent | FDA class 1 | Ear, Nose, Throat |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (ETF), ordered by most recent decision date.
JEDMED SPECTRUM ENT CABINET
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PREMIER MIRROR WARMER
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
LANGGASSE 90
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCES
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
MOBILE TREATMENT CART
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat