FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Miscellaneous
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
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
K
98
4345
AROMAPATCH
1
Cleared 510(K)
K
93
2522
AMSCO STERILE RECOVERIES SURGICAL PACKS
1
Cleared 510(K)
K
94
2789
MISTASSIST
1
Cleared 510(K)
K
94
0133
THE EXPANDACELL EAR PACK
1
Cleared 510(K)
K
92
5022
SURGICAL TRAY (STERILE)
1
Cleared 510(K)
K
92
0842
AEROSOL DELIVERY SYSTEMS
1
Cleared 510(K)
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 6 December 2024 at 11:05 pm
EN
/
subpart-f—therapeutic-devices
/
LRD
/
K925022
View Source
SURGICAL TRAY (STERILE)
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925022
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1993
Days to Decision
214 days
Submission Type
Statement
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
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
K
98
4345
AROMAPATCH
K
93
2522
AMSCO STERILE RECOVERIES SURGICAL PACKS
K
94
2789
MISTASSIST
K
94
0133
THE EXPANDACELL EAR PACK
K
92
5022
SURGICAL TRAY (STERILE)
K
92
0842
AEROSOL DELIVERY SYSTEMS
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
/
LRD
/
K925022
View Source
SURGICAL TRAY (STERILE)
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925022
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1993
Days to Decision
214 days
Submission Type
Statement