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FDA 510(k)

INJECTION SITE, CODE NO. 3100

K-Number: K800786 · 1980-05-08

ApplicantQuest Medical, Inc.
Decision Date1980-05-08
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INJECTION SITE, CODE NO. 3100 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 1980-05-08 under 510(k) number K800786. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTION SITE, CODE NO. 3100?

INJECTION SITE, CODE NO. 3100 is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Quest Medical, Inc.. The 510(k) number is K800786.

When did INJECTION SITE, CODE NO. 3100 receive FDA 510(k) clearance?

INJECTION SITE, CODE NO. 3100 received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800786.

Who is the listed applicant for INJECTION SITE, CODE NO. 3100?

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 INJECTION SITE, CODE NO. 3100?

The FDA product code for INJECTION SITE, CODE NO. 3100 is FOZ.

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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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