FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

SHAWNEE PRODUCT KIT IV

K Number: K923319 · Decision Jun 17, 1993
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
3
Review Days
345

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
SHAWNEE PRODUCT KIT IV
K Number
K923319
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Absentee Shawnee Bandage Group
Date Received
July 7, 1992
Decision Date
June 17, 1993
Product Code
KGX
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KGX Tape And Bandage, Adhesive

Similar 510(k) Clearances

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

View all

Other Clearances by Absentee Shawnee Bandage Group

K Number Device Name
K921761 SHAWNEE PRODUCTS KIT II
K921762 SHAWNEE PRODUCTS KIT I