FDA 510(k)
FDA class 1
Substantially Equivalent
🇬🇧 United Kingdom
SUNDERLAND NASAL TUBE
K Number: K883668
·
Decision Nov 21, 1988
Classifications
1
FEI Numbers
122
Registration Numbers
122
Same Product Code
18
Applicant Total
43
Review Days
87
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Basic Information
- Device Name
- SUNDERLAND NASAL TUBE
- K Number
- K883668
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5100
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Exmoor Plastics , Ltd.
- Date Received
- August 26, 1988
- Decision Date
- November 21, 1988
- Product Code
- BTQ
- 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 |
|---|---|---|---|
| BTQ | Airway, Nasopharyngeal | FDA class 1 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BTQ), ordered by most recent decision date.
AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGS
FDA 510(k)
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NASOPHARYNGEAL AIRWAY
FDA 510(k)
FDA Class 1
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NORTEC ROBERTAZZI NASOPHARYNGEAL AIRWAY
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ROBERTAZZI NASOPHARYNGEAL AIRWAY
FDA 510(k)
FDA Class 1
·Anesthesiology
POLAMEDCO NASOPAHARYNGEAL AIRWAY
FDA 510(k)
FDA Class 1
·Anesthesiology
CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY
FDA 510(k)
FDA Class 1
·Anesthesiology
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| K974008 | PFLEIDERER'S INTRATYMPANIC CATHETER | May 13, 1998 | Substantially Equivalent |
| K974224 | ENDOLYMPHATIC SAC TO MASTOID T-SHUNT | Jan 27, 1998 | Substantially Equivalent |
| K973587 | EXMOOR TYMPANOCENTESIS KIT (TK/1) | Jan 23, 1998 | Substantially Equivalent |