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FDA 510(k)

PFT FILTER

K-Number: K952062 · 1995-06-08

ApplicantIntertech Resources, Inc.
Decision Date1995-06-08
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PFT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1995-06-08 under 510(k) number K952062. 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 PFT FILTER?

PFT FILTER is a medical device that received FDA 510(k) clearance on 1995-06-08. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K952062.

When did PFT FILTER receive FDA 510(k) clearance?

PFT FILTER received FDA 510(k) clearance on 1995-06-08, under 510(k) number K952062.

Who is the listed applicant for PFT FILTER?

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

What is the FDA product code for PFT FILTER?

The FDA product code for PFT FILTER is CAH.

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Other records listing Intertech Resources, Inc. as applicant

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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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