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FDA 510(k)

HMB-200

K-Number: K800250 · 1980-03-25

ApplicantAssociated Mills, Inc.
Decision Date1980-03-25
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HMB-200 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 1980-03-25 under 510(k) number K800250. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HMB-200?

HMB-200 is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Associated Mills, Inc.. The 510(k) number is K800250.

When did HMB-200 receive FDA 510(k) clearance?

HMB-200 received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800250.

Who is the listed applicant for HMB-200?

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 HMB-200?

The FDA product code for HMB-200 is IRO.

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Related Devices (Code: IRO)

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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