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

REXTON HS(HEARING SYSTEM)

K Number: K791548 · Decision Sep 28, 1979
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
70
Applicant Total
14
Review Days
46

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Basic Information

Device Name
REXTON HS(HEARING SYSTEM)
K Number
K791548
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3690
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Argosy Intl. (Usa), Inc.
Date Received
August 13, 1979
Decision Date
September 28, 1979
Product Code
HSD
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

Similar 510(k) Clearances

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

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Other Clearances by Argosy Intl. (Usa), Inc.

K Number Device Name
K823075 REXTON
K781095 HEARING AID, BEHIND THE EAR
K781094 HEARING AID, EYEGLASS
K781096 HEARING AID, EYEGLASS, B-12
K780921 MM-CE DM (BEHIND THE EAR)
K780914 PM 25 PP (BODY AID)
K780920 MM-CE 11 (BEHIND THE EAR)
K780916 780 UE (BEHIND THE EAR)
K780917 PRIMO CE (BEHIND THE EAR)
K780915 780 SE (BEHIND THE EAR)
Search all 14 clearances from Argosy Intl. (Usa), Inc. →