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FDA 510(k)

EXTENSION SET QUEST CODE #3000

K-Number: K800825 · 1980-05-14

Decision Date1980-05-14
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXTENSION SET QUEST CODE #3000 is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800825. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENSION SET QUEST CODE #3000?

EXTENSION SET QUEST CODE #3000 is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Quest Medical, Inc.. The 510(k) number is K800825.

When did EXTENSION SET QUEST CODE #3000 receive FDA 510(k) clearance?

EXTENSION SET QUEST CODE #3000 received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800825.

Who is the listed applicant for EXTENSION SET QUEST CODE #3000?

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

What is the FDA product code for EXTENSION SET QUEST CODE #3000?

The FDA product code for EXTENSION SET QUEST CODE #3000 is FPK.

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 Quest Medical, 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 38 devices →

Related Devices (Code: FPK)

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

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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