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FDA 510(k)

6-435 FILTER PAD, 5/PKG.

K-Number: K802914 · 1980-12-19

Decision Date1980-12-19
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

6-435 FILTER PAD, 5/PKG. is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare Services, Inc.. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802914. 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 6-435 FILTER PAD, 5/PKG.?

6-435 FILTER PAD, 5/PKG. is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Lifecare Services, Inc.. The 510(k) number is K802914.

When did 6-435 FILTER PAD, 5/PKG. receive FDA 510(k) clearance?

6-435 FILTER PAD, 5/PKG. received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802914.

Who is the listed applicant for 6-435 FILTER PAD, 5/PKG.?

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

What is the FDA product code for 6-435 FILTER PAD, 5/PKG.?

The FDA product code for 6-435 FILTER PAD, 5/PKG. 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 Lifecare Services, 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 20 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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