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FDA 510(k)

DNA FLOR

K-Number: K831408 · 1983-07-28

ApplicantMedastat Scientific Corp.
Decision Date1983-07-28
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DNA FLOR is the device name listed in this FDA 510(k) record. The listed applicant is Medastat Scientific Corp.. It received FDA 510(k) clearance on 1983-07-28 under 510(k) number K831408. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DNA FLOR?

DNA FLOR is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Medastat Scientific Corp.. The 510(k) number is K831408.

When did DNA FLOR receive FDA 510(k) clearance?

DNA FLOR received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831408.

Who is the listed applicant for DNA FLOR?

The FDA 510(k) record lists Medastat Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DNA FLOR?

The FDA product code for DNA FLOR is DHN.

Other records listing Medastat Scientific Corp. 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.

K931849PARAPREPK822604ACID FAST QUALITY CONTROL SLIDES

Related Devices (Code: DHN)

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.

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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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