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FDA 510(k)

1.2 MICRON FINAL FILTER WITH EXTENSION TUBE

K-Number: K940293 · 1994-03-28

Decision Date1994-03-28
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

1.2 MICRON FINAL FILTER WITH EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Puritas Health Care, Inc.. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K940293. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1.2 MICRON FINAL FILTER WITH EXTENSION TUBE?

1.2 MICRON FINAL FILTER WITH EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K940293.

When did 1.2 MICRON FINAL FILTER WITH EXTENSION TUBE receive FDA 510(k) clearance?

1.2 MICRON FINAL FILTER WITH EXTENSION TUBE received FDA 510(k) clearance on 1994-03-28, under 510(k) number K940293.

Who is the listed applicant for 1.2 MICRON FINAL FILTER WITH EXTENSION TUBE?

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

What is the FDA product code for 1.2 MICRON FINAL FILTER WITH EXTENSION TUBE?

The FDA product code for 1.2 MICRON FINAL FILTER WITH EXTENSION TUBE is FPB.

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 Puritas Health Care, 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.

View all 24 devices →

Related Devices (Code: FPB)

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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