FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STARLIGHT

K Number: K090587 · Decision Jul 17, 2009
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
22
Applicant Total
21
Review Days
135

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Basic Information

Device Name
STARLIGHT
K Number
K090587
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5970
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthomerica Products, Inc.
Date Received
March 4, 2009
Decision Date
July 17, 2009
Product Code
OAN
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAN Orthosis, Cranial, Laser Scan

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OAN), ordered by most recent decision date.

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Other Clearances by Orthomerica Products, Inc.

K Number Device Name
K240466 STARband 3D
K223238 STARband 3D
K211376 STARband
K203098 STARband, STARlight, St. Louis Band
K180109 STARband, STARlight, St. Louis Band
K161138 St. Louis Band
K151979 STARband, STARlight
K151147 STARband, STARlight
K142141 STARBAND, STARLIGHT
K141842 STARBAND, STARLIGHT
Search all 21 clearances from Orthomerica Products, Inc. →