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FDA 510(k)

TUMORIMETER

K-Number: K874352 · 1987-11-23

ApplicantCancer Technologies, Inc.
Decision Date1987-11-23
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TUMORIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Cancer Technologies, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874352. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUMORIMETER?

TUMORIMETER is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Cancer Technologies, Inc.. The 510(k) number is K874352.

When did TUMORIMETER receive FDA 510(k) clearance?

TUMORIMETER received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874352.

Who is the listed applicant for TUMORIMETER?

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

What is the FDA product code for TUMORIMETER?

The FDA product code for TUMORIMETER is FTY.

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Other records listing Cancer Technologies, 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.

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Related Devices (Code: FTY)

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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