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FDA 510(k)

VISCOPE, MODEL 100P,100S

K-Number: K100531 · 2010-07-21

Decision Date2010-07-21
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VISCOPE, MODEL 100P,100S is the device name listed in this FDA 510(k) record. The listed applicant is Hd Medical Services (India) Pvt.Ltd. It received FDA 510(k) clearance on 2010-07-21 under 510(k) number K100531. 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 VISCOPE, MODEL 100P,100S?

VISCOPE, MODEL 100P,100S is a medical device that received FDA 510(k) clearance on 2010-07-21. The listed applicant is Hd Medical Services (India) Pvt.Ltd. The 510(k) number is K100531.

When did VISCOPE, MODEL 100P,100S receive FDA 510(k) clearance?

VISCOPE, MODEL 100P,100S received FDA 510(k) clearance on 2010-07-21, under 510(k) number K100531.

Who is the listed applicant for VISCOPE, MODEL 100P,100S?

The FDA 510(k) record lists Hd Medical Services (India) Pvt.Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISCOPE, MODEL 100P,100S?

The FDA product code for VISCOPE, MODEL 100P,100S 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.

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.

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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