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FDA 510(k)

DILATOR, MIZUTANI LAMINARIA TENT

K-Number: K782067 · 1979-01-03

ApplicantBritish Marketing Ent., Ltd.
Decision Date1979-01-03
Product CodeHDY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DILATOR, MIZUTANI LAMINARIA TENT is the device name listed in this FDA 510(k) record. The listed applicant is British Marketing Ent., Ltd.. It received FDA 510(k) clearance on 1979-01-03 under 510(k) number K782067. The device is classified under product code HDY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DILATOR, MIZUTANI LAMINARIA TENT?

DILATOR, MIZUTANI LAMINARIA TENT is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is British Marketing Ent., Ltd.. The 510(k) number is K782067.

When did DILATOR, MIZUTANI LAMINARIA TENT receive FDA 510(k) clearance?

DILATOR, MIZUTANI LAMINARIA TENT received FDA 510(k) clearance on 1979-01-03, under 510(k) number K782067.

Who is the listed applicant for DILATOR, MIZUTANI LAMINARIA TENT?

The FDA 510(k) record lists British Marketing Ent., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DILATOR, MIZUTANI LAMINARIA TENT?

The FDA product code for DILATOR, MIZUTANI LAMINARIA TENT is HDY.

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 British Marketing Ent., Ltd. 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.

K790032DISPOSABLE VACUUM CURETTE

Related Devices (Code: HDY)

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.

K040625ATAD ARD CATHETERAtad Developments , Ltd.K021012LAMINARIA 2MM/3MM/4MM/5MM/6MM/7MM/8MM/9MMQuality Medical Solusions, LLCK011512MMODIFICATION TO LAMINARIAA & A Medical, Inc.K955072LAMINARIACti Corp., Ltd.K892220LAMINARIA TENTBerkeley MedevicesK881295LAMINARIA CUREXHarold W. Berger Co.

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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