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FDA 510(k)

EASY CUFF

K-Number: K102704 · 2011-03-10

ApplicantJoan Spiegel, MD
Decision Date2011-03-10
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EASY CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Joan Spiegel, MD. It received FDA 510(k) clearance on 2011-03-10 under 510(k) number K102704. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY CUFF?

EASY CUFF is a medical device that received FDA 510(k) clearance on 2011-03-10. The listed applicant is Joan Spiegel, MD. The 510(k) number is K102704.

When did EASY CUFF receive FDA 510(k) clearance?

EASY CUFF received FDA 510(k) clearance on 2011-03-10, under 510(k) number K102704.

Who is the listed applicant for EASY CUFF?

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

What is the FDA product code for EASY CUFF?

The FDA product code for EASY CUFF is BSK.

Related Devices (Code: BSK)

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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