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FDA 510(k)

VITAL PEP

K-Number: K984468 · 1999-06-01

ApplicantVital Signs, Inc.
Decision Date1999-06-01
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VITAL PEP 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 1999-06-01 under 510(k) number K984468. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL PEP?

VITAL PEP is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is Vital Signs, Inc.. The 510(k) number is K984468.

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

VITAL PEP received FDA 510(k) clearance on 1999-06-01, under 510(k) number K984468.

Who is the listed applicant for VITAL PEP?

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 PEP?

The FDA product code for VITAL PEP is BWF.

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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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