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FDA 510(k)

DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE

K-Number: K903643 · 1990-12-24

ApplicantDeknatel, Inc.
Decision Date1990-12-24
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Deknatel, Inc.. It received FDA 510(k) clearance on 1990-12-24 under 510(k) number K903643. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE?

DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE is a medical device that received FDA 510(k) clearance on 1990-12-24. The listed applicant is Deknatel, Inc.. The 510(k) number is K903643.

When did DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE receive FDA 510(k) clearance?

DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE received FDA 510(k) clearance on 1990-12-24, under 510(k) number K903643.

Who is the listed applicant for DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE?

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

What is the FDA product code for DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE?

The FDA product code for DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE is GAW.

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Related Devices (Code: GAW)

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.

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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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