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

FLORET OPHTHALMIC EYE SPEAR

K Number: K830262 · Decision Apr 6, 1983
Classifications
1
FEI Numbers
77
Registration Numbers
78
Same Product Code
46
Applicant Total
22
Review Days
71

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Basic Information

Device Name
FLORET OPHTHALMIC EYE SPEAR
K Number
K830262
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4790
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Ritmed, Inc.
Date Received
January 25, 1983
Decision Date
April 6, 1983
Product Code
HOZ
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
HOZ Sponge, Ophthalmic

Similar 510(k) Clearances

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Other Clearances by Ritmed, Inc.

K Number Device Name
K833626 FLORET FOAM PREP SPONGE
K832874 ISOVIS WOUND PROTECTOR
K830270 ISOVIS WOUND PROTECTOR
K830267 FLORET SPECIAL GAUZE SPONGES
K830261 FLORET STRUNG GAUZE SPONGES
K830266 FLORET KITTNER OR K DISSECTOR
K830268 FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMIN
K830272 PROTET HOLDERS-BLOCKS & ROLL
K830264 FLORET TONSIL & ADENOID SPONGES
K830271 LAPET & LAPWALL LAPAROTOMY SPONGES
Search all 22 clearances from Ritmed, Inc. →