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Product codes
FAK
Product code FAK
Device name
Panendoscope (Gastroduodenoscope)
Medical specialty
Gastroenterology, Urology
Device class
2
Regulation number
876.1500
Review panel
GU
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Ineligible
Definition
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K812810
PENTAX FLEXIBLE DRIODENOFIBERSCOPE
Pentax Precision Instrument Corp.
1981-11-17
K760822
MODEL TX-8 PANENDOSCOPE
American Cystocope Makers, Inc.
1976-10-21