FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

SUTUREGROOVE WEIGHT SIZING SET

K Number: K003646 · Decision Feb 22, 2001
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
13
Applicant Total
9
Review Days
87

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
SUTUREGROOVE WEIGHT SIZING SET
K Number
K003646
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5700
Medical Specialty
Ophthalmic
Decision
Unknown
Statement or Summary
Statement
Applicant
Iop, Inc.
Date Received
November 27, 2000
Decision Date
February 22, 2001
Product Code
MML
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
MML Weights, Eyelid, External

Similar 510(k) Clearances

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

View all

Other Clearances by Iop, Inc.

K Number Device Name
K090078 KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT
K062252 MOLTENO3
K053622 SURGISIS OCULAR GRAFT
K010852 OSMED TISSUE EXPANDER
K994289 SUTUREGROOVE
K972143 MOA BONE / M-SPHERE
K902489 MODIFIED MOLTENO(TM) IMPLANTS
K890598 MOLTENO IMPLANT