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

ASPIRATING ENDO OCULAR PROBE W/ILLUMINATION

K Number: K921488 · Decision May 7, 1992
Classifications
1
FEI Numbers
234
Registration Numbers
235
Same Product Code
76
Applicant Total
28
Review Days
38

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Basic Information

Device Name
ASPIRATING ENDO OCULAR PROBE W/ILLUMINATION
K Number
K921488
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Surgical Technologies, Inc.
Date Received
March 30, 1992
Decision Date
May 7, 1992
Product Code
HMX
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
HMX Cannula, Ophthalmic

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Other Clearances by Surgical Technologies, Inc.

K Number Device Name
K941992 CYSTOSCOPE
K942029 ARTHROSCOPE
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K952566 OSCILFLATOR
K951918 SURGICAL TECHNOLOGIES, INC. SYRINGE
K950683 ARTHROGRAM TRAY
K946135 INFINITECH ASPIRATING LASER PROBE
K946181 INFINITECH SOFT TIP FLUTE NEEDLE
K942030 BIOPSY SCISSORS
K942482 PRESSURE MONITORING EXTENSION
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