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FDA 510(k)

THD

K-Number: K070815 · 2007-06-20

ApplicantG.F. S.R.L.
Decision Date2007-06-20
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THD is the device name listed in this FDA 510(k) record. The listed applicant is G.F. S.R.L.. It received FDA 510(k) clearance on 2007-06-20 under 510(k) number K070815. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THD?

THD is a medical device that received FDA 510(k) clearance on 2007-06-20. The listed applicant is G.F. S.R.L.. The 510(k) number is K070815.

When did THD receive FDA 510(k) clearance?

THD received FDA 510(k) clearance on 2007-06-20, under 510(k) number K070815.

Who is the listed applicant for THD?

The FDA 510(k) record lists G.F. S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THD?

The FDA product code for THD is JAF.

Related Devices (Code: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK063600VISTA AVSSummit Doppler Systems, Inc.

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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