FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
THERMUFF BAG
K Number: K920153
·
Decision Jul 1, 1992
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
3
Review Days
170
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
- THERMUFF BAG
- K Number
- K920153
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Techstyles
- Date Received
- January 13, 1992
- Decision Date
- July 1, 1992
- Product Code
- KDC
- 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 |
|---|---|---|---|
| KDC | Instrument, Surgical, Disposable | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KDC), ordered by most recent decision date.
DISPOSABLE SURGICAL SCISSORS AND FORCEPS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MANUAL SURGICAL INSTRUMENTS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DISPOSABLE CAUTERY ABRASIVE PAD
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INSTRUMENT ORGANIZER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SHUR-GRIP
FDA 510(k)
FDA Class 1
·General, Plastic Surgery