Product Code: PTY FDA class 2 21 CFR 882.1470

Computerized Cognitive Assessment Aid, Exempt

Neurology

The Computerized Cognitive Assessment Aid (Exempt) is a neurology device used to assist clinicians in assessing cognitive function, potentially aiding in the screening or monitoring of conditions such as dementia, traumatic brain injury, or other neurological disorders. Product code PTY is the Class II exempt counterpart of PKQ, exempted from the 510(k) requirement under the 21st Century Cures Act, subject to the limitations in 21 CFR 882.9. Under regulation 21 CFR 882.1470, it is a Class II device subject to general and special controls. It falls under the Neurology medical specialty and is not flagged as an implant or life-sustaining device.

510(k)s
0
FEI Numbers
41
Registration Numbers
41
Unique Applicants
0
Years Active

Basic Information

Product Code
PTY
Device Class
FDA class 2
Regulation Number
882.1470
Medical Specialty
Neurology
Review Panel
NE
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

Definition

This product code is the class II exempt counterpart of PKQ, and was exempted, subject to the limitations of exemption, under the procedures established by the 21st Century Cures Act. This device type does not require premarket notification (510(k)) to market if it does not exceed the general limitations of exemption found in 21 CFR 882.9 and the specific limitations of exemption as stated in the “Physical State” field of this product code description.

FEI Numbers

This FDA classification entry is associated with 41 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 41 registration numbers. Click on an entry to view related FDA registrations.