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FDA 510(k)

CANCER ANTIGEN CONTROL

K-Number: K924061 · 1993-02-23

Decision Date1993-02-23
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CANCER ANTIGEN CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Polymedco, Inc.. It received FDA 510(k) clearance on 1993-02-23 under 510(k) number K924061. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANCER ANTIGEN CONTROL?

CANCER ANTIGEN CONTROL is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is Polymedco, Inc.. The 510(k) number is K924061.

When did CANCER ANTIGEN CONTROL receive FDA 510(k) clearance?

CANCER ANTIGEN CONTROL received FDA 510(k) clearance on 1993-02-23, under 510(k) number K924061.

Who is the listed applicant for CANCER ANTIGEN CONTROL?

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

What is the FDA product code for CANCER ANTIGEN CONTROL?

The FDA product code for CANCER ANTIGEN CONTROL is JJY.

Related Clinical Trials

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.

Other records listing Polymedco, 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 19 devices →

Related Devices (Code: JJY)

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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