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FDA 510(k)

EMERGENCY-CLEAN UP(TM) ECP

K-Number: K880306 · 1988-05-20

Decision Date1988-05-20
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EMERGENCY-CLEAN UP(TM) ECP is the device name listed in this FDA 510(k) record. The listed applicant is Cdc Products Corp.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K880306. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERGENCY-CLEAN UP(TM) ECP?

EMERGENCY-CLEAN UP(TM) ECP is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Cdc Products Corp.. The 510(k) number is K880306.

When did EMERGENCY-CLEAN UP(TM) ECP receive FDA 510(k) clearance?

EMERGENCY-CLEAN UP(TM) ECP received FDA 510(k) clearance on 1988-05-20, under 510(k) number K880306.

Who is the listed applicant for EMERGENCY-CLEAN UP(TM) ECP?

The FDA 510(k) record lists Cdc Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERGENCY-CLEAN UP(TM) ECP?

The FDA product code for EMERGENCY-CLEAN UP(TM) ECP is EXB.

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 Cdc Products Corp. 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.

Related Devices (Code: EXB)

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

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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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