510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FRIClass I

Scale, Stand-On, Patient

21 CFR 880.2700 / General Hospital
FDA source (opens on fda.gov)

FRI is the FDA product code for Scale, Stand-On, Patient, a class I device type, regulated under 21 CFR 880.2700. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
FRI
Device name
Scale, Stand-On, Patient
Regulation
21 CFR 880.2700
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
3
Ingested recalls
2

Clearances, product code FRI

By decision year
3 clearances under product code FRI with a decision year between 1977 and 1979, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FRI by decision year
YearClearances
19772
19791

Applicants with the most clearances

Product code FRI
Applicants holding the most 510(k) clearances under product code FRI
ApplicantClearances
Sr Instruments Inc2
Acme Medical Scale Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 87 companies shown, in name order