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Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
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Review Panel
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Miscellaneous
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Neurological Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
OGP
Cricothyrotomy Kit
2
Product Code
OGV
Tracheostomy Cleaning Tray
2
Product Code
OGW
Tracheostomy Kit
2
Product Code
MYB
Pillow, Cervical (For Mild Sleep Apnea)
2
Product Code
EPN
Pump, Nebulizer, Manual
1
Product Code
EPP
Splint, Nasal
1
Product Code
K
94
2158
AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS
1
Cleared 510(K)
K
94
2724
EXTERNAL NASAL SPLINT
1
Cleared 510(K)
K
89
5502
MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT
1
Cleared 510(K)
K
89
0599
HOOD NASAL SPLINT
1
Cleared 510(K)
K
88
2244
RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT
1
Cleared 510(K)
K
87
2905
AMERICAN NASAL SPONGE
1
Cleared 510(K)
K
86
4933
'EXMOOR' SHAH & MACKAY NASAL SPLINTS
1
Cleared 510(K)
K
86
4932
'EXMOOR' CAWOOD NASAL SPLINTS
1
Cleared 510(K)
K
86
4930
'EXMOOR' ATKINS NASAL SPLINT
1
Cleared 510(K)
K
86
4934
'EXMOOR' SHAH SILICONE DISCS
1
Cleared 510(K)
K
86
3382
CANNON NASAL SPLINT
1
Cleared 510(K)
K
86
2496
MICROTEK INTRANASAL SPLINT
1
Cleared 510(K)
K
81
0738
GOODE MAGNETIC NASAL SPLINT
1
Cleared 510(K)
K
79
1681
THE DENVER SPLINT
1
Cleared 510(K)
K
79
1053
THE DENVER SPLINT
1
Cleared 510(K)
ETF
Unit, Examining/Treatment, Ent
1
Product Code
EWT
Device, Antichoke, Suction
3
Product Code
EWW
Device, Antichoke, Tongs
3
Product Code
JPW
Pump, Nebulizer, Electrically Powered
1
Product Code
KCJ
Applicator, Ent
1
Product Code
KCL
Blower, Powder, Ent
1
Product Code
KCM
Dropper, Ent
1
Product Code
KCN
Ear Wick
1
Product Code
KCO
Nasal Spray, Ent Delivery
1
Product Code
KCP
Syringe, Ent
1
Product Code
KMA
Irrigator, Powered Nasal
1
Product Code
KTH
Device, Anti-Stammering
1
Product Code
LRD
Applicator, Ent Drug
1
Product Code
PKA
External Upper Esophageal Sphincter (Ues) Compression Device
2
Product Code
Subpart G—General Hospital and Personal Use Miscellaneous Devices
CFR Sub-Part
Subpart G—Miscellaneous Devices
CFR Sub-Part
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 16 August 2024 at 11:05 pm
EN
/
subpart-f—therapeutic-devices
/
EPP
/
K862496
View Source
MICROTEK INTRANASAL SPLINT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862496
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1986
Days to Decision
13 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Miscellaneous
Subpart B—Diagnostic Devices
Subpart D—Prosthetic Devices
Subpart E—Neurological Surgical Devices
Subpart E—Surgical Devices
Subpart F—General Hospital and Personal Use Therapeutic Devices
Subpart F—Therapeutic Devices
OGP
Cricothyrotomy Kit
OGV
Tracheostomy Cleaning Tray
OGW
Tracheostomy Kit
MYB
Pillow, Cervical (For Mild Sleep Apnea)
EPN
Pump, Nebulizer, Manual
EPP
Splint, Nasal
K
94
2158
AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS
K
94
2724
EXTERNAL NASAL SPLINT
K
89
5502
MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT
K
89
0599
HOOD NASAL SPLINT
K
88
2244
RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT
K
87
2905
AMERICAN NASAL SPONGE
K
86
4933
'EXMOOR' SHAH & MACKAY NASAL SPLINTS
K
86
4932
'EXMOOR' CAWOOD NASAL SPLINTS
K
86
4930
'EXMOOR' ATKINS NASAL SPLINT
K
86
4934
'EXMOOR' SHAH SILICONE DISCS
K
86
3382
CANNON NASAL SPLINT
K
86
2496
MICROTEK INTRANASAL SPLINT
K
81
0738
GOODE MAGNETIC NASAL SPLINT
K
79
1681
THE DENVER SPLINT
K
79
1053
THE DENVER SPLINT
ETF
Unit, Examining/Treatment, Ent
EWT
Device, Antichoke, Suction
EWW
Device, Antichoke, Tongs
JPW
Pump, Nebulizer, Electrically Powered
KCJ
Applicator, Ent
KCL
Blower, Powder, Ent
KCM
Dropper, Ent
KCN
Ear Wick
KCO
Nasal Spray, Ent Delivery
KCP
Syringe, Ent
KMA
Irrigator, Powered Nasal
KTH
Device, Anti-Stammering
LRD
Applicator, Ent Drug
PKA
External Upper Esophageal Sphincter (Ues) Compression Device
Subpart G—General Hospital and Personal Use Miscellaneous Devices
Subpart G—Miscellaneous Devices
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
EN
/
subpart-f—therapeutic-devices
/
EPP
/
K862496
View Source
MICROTEK INTRANASAL SPLINT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862496
510(k) Type
Traditional
Applicant
MICROTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1986
Days to Decision
13 days