FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BICORD BY QMED

K Number: K863091 · Decision Aug 29, 1986
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
30
Applicant Total
11
Review Days
16

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
BICORD BY QMED
K Number
K863091
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Qmed, Inc.
Date Received
August 13, 1986
Decision Date
August 29, 1986
Product Code
HAM
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
HAM Apparatus, Electrosurgical

Similar 510(k) Clearances

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

View all

Other Clearances by Qmed, Inc.

K Number Device Name
K972991 MONITOR ONE NDX
K932109 PROFILOMAT
K921476 INTERP-1000
K897121 QEKG ELECTROCARDIOGRAPH
K873591 A.R.M. (ASPEN RETURN MONITOR)
K862377 QMED SELF ADHERING ELECTRODE
K861437 QMED SYSTEM 2150
K843559 KLEENIT BY QMED
K841172 MONITOR ONE
K840465 Q-MED ELECTRODE
Search all 11 clearances from Qmed, Inc. →