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FDA 510(k)

FATHOM CMP-1000

K-Number: K930051 · 1993-07-20

ApplicantFathom Ent., Inc.
Decision Date1993-07-20
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FATHOM CMP-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Fathom Ent., Inc.. It received FDA 510(k) clearance on 1993-07-20 under 510(k) number K930051. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FATHOM CMP-1000?

FATHOM CMP-1000 is a medical device that received FDA 510(k) clearance on 1993-07-20. The listed applicant is Fathom Ent., Inc.. The 510(k) number is K930051.

When did FATHOM CMP-1000 receive FDA 510(k) clearance?

FATHOM CMP-1000 received FDA 510(k) clearance on 1993-07-20, under 510(k) number K930051.

Who is the listed applicant for FATHOM CMP-1000?

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

What is the FDA product code for FATHOM CMP-1000?

The FDA product code for FATHOM CMP-1000 is IYO.

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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.

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