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FDA 510(k)

STUDIODOP VICORDER

K-Number: K071730 · 2007-12-20

ApplicantSkidmore Medical, Limited
Decision Date2007-12-20
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STUDIODOP VICORDER is the device name listed in this FDA 510(k) record. The listed applicant is Skidmore Medical, Limited. It received FDA 510(k) clearance on 2007-12-20 under 510(k) number K071730. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STUDIODOP VICORDER?

STUDIODOP VICORDER is a medical device that received FDA 510(k) clearance on 2007-12-20. The listed applicant is Skidmore Medical, Limited. The 510(k) number is K071730.

When did STUDIODOP VICORDER receive FDA 510(k) clearance?

STUDIODOP VICORDER received FDA 510(k) clearance on 2007-12-20, under 510(k) number K071730.

Who is the listed applicant for STUDIODOP VICORDER?

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

What is the FDA product code for STUDIODOP VICORDER?

The FDA product code for STUDIODOP VICORDER is JOP.

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Related Devices (Code: JOP)

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.

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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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