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FDA 510(k)

FIRSTVIEW

K-Number: K071492 · 2007-08-28

ApplicantRiverain Medical Group,Llc
Decision Date2007-08-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FIRSTVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Riverain Medical Group,Llc. It received FDA 510(k) clearance on 2007-08-28 under 510(k) number K071492. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRSTVIEW?

FIRSTVIEW is a medical device that received FDA 510(k) clearance on 2007-08-28. The listed applicant is Riverain Medical Group,Llc. The 510(k) number is K071492.

When did FIRSTVIEW receive FDA 510(k) clearance?

FIRSTVIEW received FDA 510(k) clearance on 2007-08-28, under 510(k) number K071492.

Who is the listed applicant for FIRSTVIEW?

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

What is the FDA product code for FIRSTVIEW?

The FDA product code for FIRSTVIEW is LLZ.

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Other records listing Riverain Medical Group,Llc 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.

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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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