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FDA 510(k)

RHINO-GUARD

K-Number: K911785 · 1991-10-07

ApplicantMicromedics, Inc.
Decision Date1991-10-07
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RHINO-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 1991-10-07 under 510(k) number K911785. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHINO-GUARD?

RHINO-GUARD is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is Micromedics, Inc.. The 510(k) number is K911785.

When did RHINO-GUARD receive FDA 510(k) clearance?

RHINO-GUARD received FDA 510(k) clearance on 1991-10-07, under 510(k) number K911785.

Who is the listed applicant for RHINO-GUARD?

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

What is the FDA product code for RHINO-GUARD?

The FDA product code for RHINO-GUARD is CAF.

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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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