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FDA 510(k)

HP-20, 30, 40, 50 & 60

K-Number: K841100 · 1984-03-23

Decision Date1984-03-23
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HP-20, 30, 40, 50 & 60 is the device name listed in this FDA 510(k) record. The listed applicant is Associated Mills, Inc.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K841100. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP-20, 30, 40, 50 & 60?

HP-20, 30, 40, 50 & 60 is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Associated Mills, Inc.. The 510(k) number is K841100.

When did HP-20, 30, 40, 50 & 60 receive FDA 510(k) clearance?

HP-20, 30, 40, 50 & 60 received FDA 510(k) clearance on 1984-03-23, under 510(k) number K841100.

Who is the listed applicant for HP-20, 30, 40, 50 & 60?

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

What is the FDA product code for HP-20, 30, 40, 50 & 60?

The FDA product code for HP-20, 30, 40, 50 & 60 is IRT.

Other records listing Associated Mills, Inc. 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.

View all 14 devices →

Related Devices (Code: IRT)

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.

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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