Product Code: FFR FDA class 1 21 CFR 876.4730

Device, Locking, For Intestinal Clamp

Gastroenterology, Urology

The Locking Device for Intestinal Clamp is an accessory component that secures an intestinal clamp in a fixed position during gastrointestinal surgery to prevent unintended movement. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is FFR, regulated under 21 CFR 876.4730, within the Gastroenterology, Urology specialty.

510(k)s
0
FEI Numbers
23
Registration Numbers
23
Unique Applicants
0
Years Active

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Basic Information

Product Code
FFR
Device Class
FDA class 1
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Review Panel
GU
Submission Type
4

Device Characteristics

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

FEI Numbers

This FDA classification entry is associated with 23 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 23 registration numbers. Click on an entry to view related FDA registrations.