FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
RHYTIDOMETER
K Number: K801939
·
Decision Sep 26, 1980
Classifications
1
FEI Numbers
398
Registration Numbers
398
Same Product Code
22
Applicant Total
5
Review Days
45
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
- RHYTIDOMETER
- K Number
- K801939
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Aztec Medical Products, Inc.
- Date Received
- August 12, 1980
- Decision Date
- September 26, 1980
- Product Code
- FTY
- 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 |
|---|---|---|---|
| FTY | Tape, Measuring, Rulers And Calipers | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FTY), ordered by most recent decision date.
Noxilizer Surgical Ruler
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DISPOSABLE WOUND MEASURE GUIDE, PLASTIC, PROTECTOR, WOUND, PLASTIC
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
OLYMPIC AUTO-LENGTH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
OLYMPIC INFA-LENGTH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
STRYKER PRESSURE MONITOR SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PEDIATRIC AIRWAY MEASUREMENT SYSTEM & P.A.M.S.
FDA 510(k)
FDA Class 1
·General, Plastic Surgery