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FDA 510(k)

POSIVAC

K-Number: K791127 · 1979-07-30

ApplicantVital Signs, Inc.
Decision Date1979-07-30
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POSIVAC 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 1979-07-30 under 510(k) number K791127. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSIVAC?

POSIVAC is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Vital Signs, Inc.. The 510(k) number is K791127.

When did POSIVAC receive FDA 510(k) clearance?

POSIVAC received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791127.

Who is the listed applicant for POSIVAC?

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 POSIVAC?

The FDA product code for POSIVAC is CBN.

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Other records listing Vital Signs, Inc. as applicant

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.

K112902ENFLOW IV FLUID WARMERK041309IMASK TMK030985BREAS PV 10I CPAP SYSTEM, MODEL PV 10IK022402DISPOSABLE PRESSURE MANOMETERK021315SURE-LOKK002454BREAS HA50 HUMIDIFIER, MODEL HA50

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Related Devices (Code: CBN)

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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