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FDA 510(k)

MEDICAL ASSEMBLIES FILTER

K-Number: K911738 · 1991-07-11

ApplicantMedical Assemblies, Inc.
Decision Date1991-07-11
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDICAL ASSEMBLIES FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Assemblies, Inc.. It received FDA 510(k) clearance on 1991-07-11 under 510(k) number K911738. 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 MEDICAL ASSEMBLIES FILTER?

MEDICAL ASSEMBLIES FILTER is a medical device that received FDA 510(k) clearance on 1991-07-11. The listed applicant is Medical Assemblies, Inc.. The 510(k) number is K911738.

When did MEDICAL ASSEMBLIES FILTER receive FDA 510(k) clearance?

MEDICAL ASSEMBLIES FILTER received FDA 510(k) clearance on 1991-07-11, under 510(k) number K911738.

Who is the listed applicant for MEDICAL ASSEMBLIES FILTER?

The FDA 510(k) record lists Medical Assemblies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAL ASSEMBLIES FILTER?

The FDA product code for MEDICAL ASSEMBLIES 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.

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Other records listing Medical Assemblies, 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.

K911737MEDICAL ASSEMBLIES MASS SPECT MONIT LINE/CONNECTK911736MEDICAL ASSEMBLIES ADULT ANESTHESIA BREATH CIRCUIT

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

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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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