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FDA 510(k)

SUTUREGROOVE WEIGHT SIZING SET

K-Number: K003646 · 2001-02-22

ApplicantIop, Inc.
Decision Date2001-02-22
Product CodeMML
Advisory CommitteeOP
DecisionUnknown

Device Summary

SUTUREGROOVE WEIGHT SIZING SET is the device name listed in this FDA 510(k) record. The listed applicant is Iop, Inc.. It received FDA 510(k) clearance on 2001-02-22 under 510(k) number K003646. The device is classified under product code MML. It was reviewed by the OP advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUTUREGROOVE WEIGHT SIZING SET?

SUTUREGROOVE WEIGHT SIZING SET is a medical device that received FDA 510(k) clearance on 2001-02-22. The listed applicant is Iop, Inc.. The 510(k) number is K003646.

When did SUTUREGROOVE WEIGHT SIZING SET receive FDA 510(k) clearance?

SUTUREGROOVE WEIGHT SIZING SET received FDA 510(k) clearance on 2001-02-22, under 510(k) number K003646.

Who is the listed applicant for SUTUREGROOVE WEIGHT SIZING SET?

The FDA 510(k) record lists Iop, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTUREGROOVE WEIGHT SIZING SET?

The FDA product code for SUTUREGROOVE WEIGHT SIZING SET is MML.

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Other records listing Iop, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K090078KERASYS BIOENGINEERED LAMELLAR PATCH GRAFTK062252MOLTENO3K053622SURGISIS OCULAR GRAFTK010852OSMED TISSUE EXPANDERK994289SUTUREGROOVEK972143MOA BONE / M-SPHERE

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Related Devices (Code: MML)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K170591Altomed Malhotra Platinum SegmentsAltomed LimitedK021750LID CHAIN EYELID WEIGHTSJedmed Instrument Co.K011740CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)Meddev Corp.K011115KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010Heinz Kurz GmbH MedizintechnikK001123KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111Heinz Kurz GmbH MedizintechnikK994289SUTUREGROOVEIop, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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