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FDA 510(k)

TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)

K-Number: K051573 · 2006-06-26

ApplicantDr. Howard Martin, P.A.
Decision Date2006-06-26
Product CodeEKM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Howard Martin, P.A.. It received FDA 510(k) clearance on 2006-06-26 under 510(k) number K051573. The device is classified under product code EKM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)?

TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) is a medical device that received FDA 510(k) clearance on 2006-06-26. The listed applicant is Dr. Howard Martin, P.A.. The 510(k) number is K051573.

When did TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) receive FDA 510(k) clearance?

TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) received FDA 510(k) clearance on 2006-06-26, under 510(k) number K051573.

Who is the listed applicant for TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)?

The FDA 510(k) record lists Dr. Howard Martin, P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)?

The FDA product code for TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) is EKM.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dr. Howard Martin, P.A. 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.

K973636MCS-MEDICATED CANAL SEALERK971641ANTIBACTERIAL GUTTA PERCHA

Related Devices (Code: EKM)

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.

K073369EI DOWNPAK BARRIER SLEEVESHu-Friedy Mfg. Co., Inc.K070246DOWN PAKEndo Twinn B.V.K042870ENDO TWINNEndo Twinn B.V.K023819FIBERFILL SGPPentron Clinical TechnologiesK971641ANTIBACTERIAL GUTTA PERCHADr. Howard Martin, P.A.K970134THERMAPREP PLUS OVENTulsa Dental Products, Ltd.

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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