FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SUCTION CANNULAS
K Number: K841249
·
Decision Jun 4, 1984
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
4
Review Days
75
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
- SUCTION CANNULAS
- K Number
- K841249
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Custom Surgical Products, Inc.
- Date Received
- March 21, 1984
- Decision Date
- June 4, 1984
- Product Code
- GEA
- 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 |
|---|---|---|---|
| GEA | Cannula, Surgical, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GEA), ordered by most recent decision date.
MRI SAFE INSTRUMENTS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
GENICON TROCAR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CONMED TROGARD ELECTRONIC TROCAR SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ORIGIN SECONDARY CANNULA AND TROCAR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery