FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SURGICAL EYE PACK

K Number: K851906 · Decision May 21, 1985
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
16
Applicant Total
9
Review Days
20

Basic Information

Device Name
SURGICAL EYE PACK
K Number
K851906
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4440
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Xanmed Corp.
Date Received
May 1, 1985
Decision Date
May 21, 1985
Product Code
HMP
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
HMP Pad, Eye

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Other Clearances by Xanmed Corp.

K Number Device Name
K864623 OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT
K844595 ORTHOPEDIC CUSTOM SURGICAL KIT
K844596 EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT
K844593 CARDIOVASCULAR CUSTOM SURGICAL KIT
K844594 NEURO CUSTOM SURGICAL KIT
K844597 MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT
K843642 SUBCLAVIAN LEAD INTRODUCER SYS
K843641 CATHETER INTRODUCER SYSTEM