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FDA 510(k)

BREATHING CIRCUIT BACTERIA FILTER

K-Number: K831856 · 1983-09-26

ApplicantVital Signs, Inc.
Decision Date1983-09-26
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BREATHING CIRCUIT BACTERIA FILTER 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 1983-09-26 under 510(k) number K831856. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BREATHING CIRCUIT BACTERIA FILTER?

BREATHING CIRCUIT BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Vital Signs, Inc.. The 510(k) number is K831856.

When did BREATHING CIRCUIT BACTERIA FILTER receive FDA 510(k) clearance?

BREATHING CIRCUIT BACTERIA FILTER received FDA 510(k) clearance on 1983-09-26, under 510(k) number K831856.

Who is the listed applicant for BREATHING CIRCUIT BACTERIA FILTER?

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 BREATHING CIRCUIT BACTERIA FILTER?

The FDA product code for BREATHING CIRCUIT BACTERIA FILTER is CAH.

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Related Devices (Code: CAH)

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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