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FDA 510(k)

SENSORMEDICS MICROGARD MICROBIAL FILTER

K-Number: K934272 · 1993-11-24

Decision Date1993-11-24
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSORMEDICS MICROGARD MICROBIAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Sensor Medics Corp.. It received FDA 510(k) clearance on 1993-11-24 under 510(k) number K934272. 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 SENSORMEDICS MICROGARD MICROBIAL FILTER?

SENSORMEDICS MICROGARD MICROBIAL FILTER is a medical device that received FDA 510(k) clearance on 1993-11-24. The listed applicant is Sensor Medics Corp.. The 510(k) number is K934272.

When did SENSORMEDICS MICROGARD MICROBIAL FILTER receive FDA 510(k) clearance?

SENSORMEDICS MICROGARD MICROBIAL FILTER received FDA 510(k) clearance on 1993-11-24, under 510(k) number K934272.

Who is the listed applicant for SENSORMEDICS MICROGARD MICROBIAL FILTER?

The FDA 510(k) record lists Sensor Medics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSORMEDICS MICROGARD MICROBIAL FILTER?

The FDA product code for SENSORMEDICS MICROGARD MICROBIAL FILTER is CAH.

Related Clinical Trials

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.

Other records listing Sensor Medics Corp. 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.

View all 26 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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