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FDA 510(k)

MULTISCOPE

K-Number: K791334 · 1979-08-10

ApplicantAmdia Medical Products
Decision Date1979-08-10
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTISCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Amdia Medical Products. It received FDA 510(k) clearance on 1979-08-10 under 510(k) number K791334. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTISCOPE?

MULTISCOPE is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Amdia Medical Products. The 510(k) number is K791334.

When did MULTISCOPE receive FDA 510(k) clearance?

MULTISCOPE received FDA 510(k) clearance on 1979-08-10, under 510(k) number K791334.

Who is the listed applicant for MULTISCOPE?

The FDA 510(k) record lists Amdia Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTISCOPE?

The FDA product code for MULTISCOPE is DQD.

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 Amdia Medical Products 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.

K791333BOWLES STETHOSCOPEK791335NURSESCOPEK791338DUAL HEAD STETHOSCOPEK791337TAYLOR NEUROLOGICAL HAMMERK791336BUCKS NEUROLOGICAL HAMMER

Related Devices (Code: DQD)

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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