FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SURELOC CIRCUIT CONNECTOR
K Number: K954383
·
Decision Dec 22, 1995
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
93
Applicant Total
20
Review Days
94
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Basic Information
- Device Name
- SURELOC CIRCUIT CONNECTOR
- K Number
- K954383
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5810
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Polamedco, Inc.
- Date Received
- September 19, 1995
- Decision Date
- December 22, 1995
- Product Code
- BZA
- 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 |
|---|---|---|---|
| BZA | Connector, Airway (Extension) | FDA class 1 | Anesthesiology |
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Other Clearances by Polamedco, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K983000 | CRICOTHYROTOMY TUBE | Oct 27, 1999 | Substantially Equivalent |
| K953793 | INTROSCOPE | Nov 29, 1995 | Substantially Equivalent |
| K950713 | AIRGUIDE STYLETTE | May 17, 1995 | Substantially Equivalent |
| K933596 | GASTRIC, CATHETER, IRRIGATION & ASPIRATION | Feb 13, 1995 | Substantially Equivalent |
| K950380 | FLEXTITIP STYLETTE | Feb 10, 1995 | Substantially Equivalent |
| K920900 | POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES | Mar 18, 1992 | Substantially Equivalent |
| K900456 | POLAMEDCO NASOPAHARYNGEAL AIRWAY | Apr 19, 1990 | Substantially Equivalent |
| K900457 | CUFFED LINDER NASOTRACHEAL AIRWAY | Apr 16, 1990 | Substantially Equivalent |
| K894516 | VISOSHIELD(TM), SURGICAL EYE PROTECTOR | Sep 12, 1989 | Substantially Equivalent |
| K881496 | LINDER NASOTRACHEAL AIRWAY | May 31, 1988 | Substantially Equivalent |