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

Picore

K Number: K212082 · Decision Oct 6, 2021
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
10
Review Days
96

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
Picore
K Number
K212082
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Med USA, Inc.
Date Received
July 2, 2021
Decision Date
October 6, 2021
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

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

View all

Other Clearances by Bio-Med USA, Inc.

K Number Device Name
K221789 IRIS Pi Q switched Nd YAG laser
K182270 Cellene CO2 Laser System
K163638 Dental 5 Multi Diode laser
K140837 LUCID LY
K133774 ATOVEN
K123710 UNITOX BOTOX SYRINGE
K121268 WANDY DISPERSVIE ELECTRODE
K111831 MX-7000 MICROXEL
K081547 BIO-MED SOFT INSULIN SYRINGE: MODELS 1CC, 0.5CC, 0.3CC