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FDA 510(k)

BSINUS DIAPHANOGRAPH

K-Number: K827448 · 1982-05-19

ApplicantSinus Medical, Inc.
Decision Date1982-05-19
Product Code
DecisionSubstantially Equivalent

Device Summary

BSINUS DIAPHANOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Sinus Medical, Inc.. It received FDA 510(k) clearance on 1982-05-19 under 510(k) number K827448. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BSINUS DIAPHANOGRAPH?

BSINUS DIAPHANOGRAPH is a medical device that received FDA 510(k) clearance on 1982-05-19. The listed applicant is Sinus Medical, Inc.. The 510(k) number is K827448.

When did BSINUS DIAPHANOGRAPH receive FDA 510(k) clearance?

BSINUS DIAPHANOGRAPH received FDA 510(k) clearance on 1982-05-19, under 510(k) number K827448.

Who is the listed applicant for BSINUS DIAPHANOGRAPH?

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

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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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