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

PENLIGHT/SWAB HOLDER

K Number: K791001 · Decision Jun 22, 1979
Classifications
1
FEI Numbers
156
Registration Numbers
156
Same Product Code
5
Applicant Total
83
Review Days
24

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
PENLIGHT/SWAB HOLDER
K Number
K791001
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6350
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
May 29, 1979
Decision Date
June 22, 1979
Product Code
KYT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KYT Light, Examination, Medical, Battery Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Concept, Inc.

K Number Device Name
K912640 CONCEPT ENDOSTEAL FIXATION DEVICE
K912957 CONCEPT MICROMILL
K896648 CONCEPT UNICOMPARTMENTAL KNEE SYSTEM
K894929 STAPLE FIXATION SYSTEM
K892376 INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)
K891109 PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
K881954 CONCEPT POWER SYSTEM
K884255 CONCEPT CCT-5200, THERMAL THERAPY SYSTEM
K882121 C-FLO SUCTION TUBE
K880414 TENDON HARVESTER
Search all 83 clearances from Concept, Inc. →