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FDA 510(k)

CUFF-ABLE PLUS

K-Number: K990412 · 1999-09-01

ApplicantVital Signs, Inc.
Decision Date1999-09-01
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CUFF-ABLE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1999-09-01 under 510(k) number K990412. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUFF-ABLE PLUS?

CUFF-ABLE PLUS is a medical device that received FDA 510(k) clearance on 1999-09-01. The listed applicant is Vital Signs, Inc.. The 510(k) number is K990412.

When did CUFF-ABLE PLUS receive FDA 510(k) clearance?

CUFF-ABLE PLUS received FDA 510(k) clearance on 1999-09-01, under 510(k) number K990412.

Who is the listed applicant for CUFF-ABLE PLUS?

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

What is the FDA product code for CUFF-ABLE PLUS?

The FDA product code for CUFF-ABLE PLUS is DXQ.

Other records listing Vital Signs, Inc. as applicant

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Related Devices (Code: DXQ)

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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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