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FDA 510(k)

VITAL PAK

K-Number: K955417 · 1996-03-08

ApplicantVital Signs, Inc.
Decision Date1996-03-08
Product CodeDXG
Advisory CommitteeCV
DecisionUnknown

Device Summary

VITAL PAK 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 1996-03-08 under 510(k) number K955417. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VITAL PAK?

VITAL PAK is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Vital Signs, Inc.. The 510(k) number is K955417.

When did VITAL PAK receive FDA 510(k) clearance?

VITAL PAK received FDA 510(k) clearance on 1996-03-08, under 510(k) number K955417.

Who is the listed applicant for VITAL PAK?

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 VITAL PAK?

The FDA product code for VITAL PAK is DXG.

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Other records listing Vital Signs, Inc. as applicant

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Related Devices (Code: DXG)

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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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