FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AIK-100 ANESTHESIA INDUCTION KIT/TRAY
K Number: K874674
·
Decision Mar 2, 1988
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
5
Review Days
110
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
- AIK-100 ANESTHESIA INDUCTION KIT/TRAY
- K Number
- K874674
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5140
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Medical Repackers Co.
- Date Received
- November 13, 1987
- Decision Date
- March 2, 1988
- Product Code
- CAZ
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (CAZ), ordered by most recent decision date.
Arrow 0.2 Micron Flat Filter, GVS
FDA 510(k)
FDA Class 2
·Anesthesiology
BD Epilor Syringe
FDA 510(k)
FDA Class 2
·Anesthesiology
Plastic LOR Syringe
FDA 510(k)
FDA Class 2
·Anesthesiology
E-Cath STIM acc. Tsui
FDA 510(k)
FDA Class 2
·Anesthesiology
VPC
FDA 510(k)
FDA Class 2
·Anesthesiology
Arrow Epidural Catheter Kit
FDA 510(k)
FDA Class 2
·Anesthesiology