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FDA 510(k)

EXTENSION SETS WITH AND WITHOUT FILTERS

K-Number: K890176 · 1989-04-26

Decision Date1989-04-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTENSION SETS WITH AND WITHOUT FILTERS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Support Systems. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K890176. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION SETS WITH AND WITHOUT FILTERS?

EXTENSION SETS WITH AND WITHOUT FILTERS is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Medical Support Systems. The 510(k) number is K890176.

When did EXTENSION SETS WITH AND WITHOUT FILTERS receive FDA 510(k) clearance?

EXTENSION SETS WITH AND WITHOUT FILTERS received FDA 510(k) clearance on 1989-04-26, under 510(k) number K890176.

Who is the listed applicant for EXTENSION SETS WITH AND WITHOUT FILTERS?

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

What is the FDA product code for EXTENSION SETS WITH AND WITHOUT FILTERS?

The FDA product code for EXTENSION SETS WITH AND WITHOUT FILTERS is FPA.

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 Medical Support Systems 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: FPA)

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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