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FDA 510(k)

BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE

K-Number: K010572 · 2001-03-12

ApplicantBecton, Dickinson and Co.
Decision Date2001-03-12
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Co.. It received FDA 510(k) clearance on 2001-03-12 under 510(k) number K010572. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE?

BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE is a medical device that received FDA 510(k) clearance on 2001-03-12. The listed applicant is Becton, Dickinson and Co.. The 510(k) number is K010572.

When did BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE receive FDA 510(k) clearance?

BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE received FDA 510(k) clearance on 2001-03-12, under 510(k) number K010572.

Who is the listed applicant for BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE?

The FDA 510(k) record lists Becton, Dickinson and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE?

The FDA product code for BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE is KKX.

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Related Devices (Code: KKX)

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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