FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
LASER SHIELDING TUBE
K Number: K894669
·
Decision Oct 13, 1989
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
7
Review Days
81
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Basic Information
- Device Name
- LASER SHIELDING TUBE
- K Number
- K894669
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5730
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Vitaid, Ltd.
- Date Received
- July 24, 1989
- Decision Date
- October 13, 1989
- Product Code
- BTR
- 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 |
|---|---|---|---|
| BTR | Tube, Tracheal (W/Wo Connector) | FDA class 2 | Anesthesiology |
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Other Clearances by Vitaid, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K050803 | PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES | Jun 30, 2005 | Substantially Equivalent |
| K932647 | WIRE REINFORCED ENDOTRACHEAL TUBE | Nov 2, 1993 | Substantially Equivalent |
| K901738 | SELFCATH | Jun 27, 1990 | Substantially Equivalent |
| K894883 | PHYCON ALL SILICONE BALLOON CATHETER | Apr 25, 1990 | Substantially Equivalent |
| K894794 | AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP | Nov 21, 1989 | Substantially Equivalent |
| K894337 | UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM | Sep 29, 1989 | Substantially Equivalent |