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FDA 510(k)

MODIFIED ENTRAPPING FILTER

K-Number: K901476 · 1990-05-01

Decision Date1990-05-01
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED ENTRAPPING FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Cadema Medical Products, Inc.. It received FDA 510(k) clearance on 1990-05-01 under 510(k) number K901476. 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 MODIFIED ENTRAPPING FILTER?

MODIFIED ENTRAPPING FILTER is a medical device that received FDA 510(k) clearance on 1990-05-01. The listed applicant is Cadema Medical Products, Inc.. The 510(k) number is K901476.

When did MODIFIED ENTRAPPING FILTER receive FDA 510(k) clearance?

MODIFIED ENTRAPPING FILTER received FDA 510(k) clearance on 1990-05-01, under 510(k) number K901476.

Who is the listed applicant for MODIFIED ENTRAPPING FILTER?

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

What is the FDA product code for MODIFIED ENTRAPPING FILTER?

The FDA product code for MODIFIED ENTRAPPING 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 Cadema Medical Products, 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.

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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