FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FLORIO CPC BAND

K Number: K760970 · Decision Nov 23, 1976
Classifications
1
FEI Numbers
167
Registration Numbers
167
Same Product Code
3
Applicant Total
48
Review Days
19

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FLORIO CPC BAND
K Number
K760970
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Richard'S Medical Equip., Inc.
Date Received
November 4, 1976
Decision Date
November 23, 1976
Product Code
HWN
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWN Instrument, Compression

Similar 510(k) Clearances

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

View all

Other Clearances by Richard'S Medical Equip., Inc.

K Number Device Name
K830793 PATIENT GUIDED ELBOW & SHOULDER EXERC
K823837 RMC TOTAL KNEE SYSTEM
K823726 SPECTRON CONVERSION ENDOPROSTHESIS CUP
K823724 SPECTRON NECK REPLACEMENT PROSTHESIS
K823723 SPECTRON PROXIMAL FEMORAL PROSTHESIS
K823722 SPECTRON LONG, STRAIGHT FEMORAL PROSTHES
K823727 SPECTRON PRIMARY STEM FEMORAL PROSTHES
K830153 RICHARDS INTRA-ARTICULAR SHAVER BLADES
K830154 COLLES FRACTURE FRAME
K823725 SPECTRON PROTRUSIO CUP
Search all 48 clearances from Richard'S Medical Equip., Inc. →