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

FIBER OPTIC ADAPTERS#60-0893

K Number: K810300 · Decision Feb 27, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
27
Applicant Total
55
Review Days
24

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
FIBER OPTIC ADAPTERS#60-0893
K Number
K810300
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Aspen Laboratories, Inc.
Date Received
February 3, 1981
Decision Date
February 27, 1981
Product Code
HBI
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
HBI Illuminator, Fiberoptic, Surgical Field

Similar 510(k) Clearances

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

View all

Other Clearances by Aspen Laboratories, Inc.

K Number Device Name
K981220 SYSTEM 7500 ABC ELECTROSURGICAL UNIT
K963088 SHEATH, ELECTROSURGICAL PENCIL
K955834 SYSTEM 6500 ABC ELECTROSURGICAL UNIT
K960296 4000 ETM
K953081 BEAMER PLUS
K953007 EXCALIBUR PLUS ELECTROSURGICAL UNIT
K946104 SMOKIEVAC ELECTROSURGICAL PENCIL
K944012 ELECTROSURGICAL FLEXIBLE ELECTRODE IN-LINE SUCTION COAGULATOR
K924960 EXCALIBUR ELECTROSURGICAL UNIT
K913213 SINGLE USE LEE ELECTRODE
Search all 55 clearances from Aspen Laboratories, Inc. →