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

NEEDLE W/STYLET FOR IMPLANTATION

K Number: K854238 · Decision Nov 13, 1985
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
18
Review Days
23

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
NEEDLE W/STYLET FOR IMPLANTATION
K Number
K854238
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
October 21, 1985
Decision Date
November 13, 1985
Product Code
GAA
Advisory Committee
General, Plastic Surgery
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
GAA Needle, Aspiration And Injection, Disposable

Similar 510(k) Clearances

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

View all

Other Clearances by Microvasive

K Number Device Name
K872771 LOW PROFILE GASTROSTOMY
K870705 THERMAL COAGULATOR
K861309 JEJUNAL FEEDING TUBE
K861323 REPLACEMENT GASTROSTOMY TUBE
K860589 INFLATOR/DEFLATOR PISTON SYRINGE
K860366 CHALLENGER HOT BIOPSY FORCEPS
K854063 MICROVASIVE SILICONE SPRAY
K851652 PAPILLOTOME
K850393 FLEXIBLE FIBEROPTIC ENDOSCOPE
K844769 RIGID FIBEROPITC ENDOSCOPE
Search all 18 clearances from Microvasive →