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

DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS

K Number: K854118 · Decision Mar 17, 1986
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
39
Applicant Total
20
Review Days
159

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
DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS
K Number
K854118
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3730
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Dacomed Corp.
Date Received
October 9, 1985
Decision Date
March 17, 1986
Product Code
EWL
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EWL Prosthesis, Laryngeal (Taub)

Similar 510(k) Clearances

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

View all

Other Clearances by Dacomed Corp.

K Number Device Name
K953640 DUNA II PENILE PROSTHESIS
K941781 RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
K920409 DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE
K920420 DURA II PENILE PROSTHESIS
K912344 MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS
K900774 DACOMED NEGATIVE PRESSURE ERECTION DEVICE
K885323 DACOMED EXTERNAL MALE CONTINENCE DEVICE
K880391 DACOMED CYSTOMETER
K871653 DURAPHASE PENILE PROSTHESIS
K870320 DACOMED PENILE PROSTHESIS SIZER
Search all 20 clearances from Dacomed Corp. →