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FDA 510(k)

SITESCRUB IPA DEVICE

K-Number: K112791 · 2012-02-24

ApplicantC. R. Bard
Decision Date2012-02-24
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

SITESCRUB IPA DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is C. R. Bard. It received FDA 510(k) clearance on 2012-02-24 under 510(k) number K112791. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITESCRUB IPA DEVICE?

SITESCRUB IPA DEVICE is a medical device that received FDA 510(k) clearance on 2012-02-24. The listed applicant is C. R. Bard. The 510(k) number is K112791.

When did SITESCRUB IPA DEVICE receive FDA 510(k) clearance?

SITESCRUB IPA DEVICE received FDA 510(k) clearance on 2012-02-24, under 510(k) number K112791.

Who is the listed applicant for SITESCRUB IPA DEVICE?

The FDA 510(k) record lists C. R. Bard as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SITESCRUB IPA DEVICE?

The FDA product code for SITESCRUB IPA DEVICE is LKB.

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Related Devices (Code: LKB)

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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