FDA 510(k)

RAHD 3100

K-Number: K903313 · 1991-10-07

Decision Date1991-10-07

Product CodeKPQ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

RAHD 3100 is the device name listed in this FDA 510(k) record. The listed applicant is Esm , Ltd.. It received FDA 510(k) clearance on 1991-10-07 under 510(k) number K903313. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAHD 3100?

RAHD 3100 is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is Esm , Ltd.. The 510(k) number is K903313.

When did RAHD 3100 receive FDA 510(k) clearance?

RAHD 3100 received FDA 510(k) clearance on 1991-10-07, under 510(k) number K903313.

Who is the listed applicant for RAHD 3100?

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

What is the FDA product code for RAHD 3100?

The FDA product code for RAHD 3100 is KPQ.

Related Devices (Code: KPQ)

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.