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

XOMED THERMAL MYRINGOTOMY SYSTEM

K Number: K820157 · Decision Mar 2, 1982
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
23
Applicant Total
82
Review Days
42

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
XOMED THERMAL MYRINGOTOMY SYSTEM
K Number
K820157
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4115
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Xomed, Inc.
Date Received
January 19, 1982
Decision Date
March 2, 1982
Product Code
HQP
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HQP Unit, Cautery, Thermal, Battery-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Xomed, Inc.

K Number Device Name
K002395 MODEL 30 CLASSIC PNEUMATONOMETER
K002987 REDTRONIC XOMED MONOPOLAR ENERGIZED BLADE
K002828 XPS NITRO SYSTEM
K002897 TITANIUM MIDDLE EAR PROSTHESES
K993653 MICRO-FRANCE TROCARS AND ACCESSORIES
K001148 MEROGEL OTOLOGIC PACK
K994262 FRONTAL SINUS TREPHINATION CANNULA
K992855 XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
K993582 MODIFICATION TO LASER-SHIELD II
K993655 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
Search all 82 clearances from Xomed, Inc. →