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FDA 510(k)

COMPUTRIM 900

K-Number: K800939 · 1980-05-28

ApplicantAmf, Inc.
Decision Date1980-05-28
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMPUTRIM 900 is the device name listed in this FDA 510(k) record. The listed applicant is Amf, Inc.. It received FDA 510(k) clearance on 1980-05-28 under 510(k) number K800939. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUTRIM 900?

COMPUTRIM 900 is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Amf, Inc.. The 510(k) number is K800939.

When did COMPUTRIM 900 receive FDA 510(k) clearance?

COMPUTRIM 900 received FDA 510(k) clearance on 1980-05-28, under 510(k) number K800939.

Who is the listed applicant for COMPUTRIM 900?

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

What is the FDA product code for COMPUTRIM 900?

The FDA product code for COMPUTRIM 900 is ISD.

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Related Devices (Code: ISD)

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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