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

COMPOUND W FREEZE OFF WART REMOVAL SYSTEM

K Number: K060859 · Decision Jul 18, 2006
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
261
Applicant Total
30
Review Days
112

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
COMPOUND W FREEZE OFF WART REMOVAL SYSTEM
K Number
K060859
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4350
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OraSure Technologies, Inc.
Date Received
March 28, 2006
Decision Date
July 18, 2006
Product Code
GEH
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
GEH Unit, Cryosurgical, Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by OraSure Technologies, Inc.

K Number Device Name
DEN190025 OraQuick Ebola Rapid Antigen Test
K023487 HISTOFREEZER WART REMOVAL SYSTEM OR OTHER PROPRIETARY NAME
K013882 OTI BENZODIAZEPINES INTERCEPT MICRO-PLATE EIA MODEL #1110I
K020371 UPLINK TEST SYSTEM
K011057 INTERCEPT ORAL FLUID DRUG TEST ORAL SPECIMEN COLLECTION DEVICE, MODEL 503-XXXX
K002375 STC CANNABINOIDS INTERCEPT MICRO-PLATE EIA, MODEL 1118I
K001976 STC BARBITURATES INTERCEPT MICRO-PLATE EIA, MODEL 1108I
K002010 STC METHADONE INTERCEPT MICRO-PLATE EIA, MODEL 11421
K000399 STC PCP INTERCEPT MICRO-PLATE EIA, MODEL 11541
K001197 COCAINE METABOLITE INTERCEPT MICRO-PLATE EIA
Search all 30 clearances from OraSure Technologies, Inc. →