FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SERENE WRAP

K Number: K895865 · Decision Dec 27, 1989
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
27
Review Days
86

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
SERENE WRAP
K Number
K895865
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Byron Medical
Date Received
October 2, 1989
Decision Date
December 27, 1989
Product Code
EFQ
Advisory Committee
Unknown
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
EFQ Gauze/Sponge, Internal

Similar 510(k) Clearances

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

View all

Other Clearances by Byron Medical

K Number Device Name
K040149 PSI-TEC PERISTALTIC INFILTRATION PUMP
K001803 ACCELERATOR RECIPROCATING CANNULA
K981215 PSI-TEC LIPOSUCTION ASPIRATOR
K981172 LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES
K980738 PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID IRRIGAION/INFILTRATION
K980392 PSI-TEC ASPIRATOR
K974295 BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING
K973133 BIG BAG 3000 PRESSURE INFUSOR
K934179 DISPOSABLE BAG DECANTER
K934233 ZARA ZONE IV MALAR IMPLANT MODIFICATION
Search all 27 clearances from Byron Medical →