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FDA 510(k)

THE MCP-70-SE SYSTEM

K-Number: K844180 · 1985-02-01

ApplicantEllis Pharmaceutical Consulting, Inc.
Decision Date1985-02-01
Product CodeKQA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THE MCP-70-SE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. It received FDA 510(k) clearance on 1985-02-01 under 510(k) number K844180. The device is classified under product code KQA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MCP-70-SE SYSTEM?

THE MCP-70-SE SYSTEM is a medical device that received FDA 510(k) clearance on 1985-02-01. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. The 510(k) number is K844180.

When did THE MCP-70-SE SYSTEM receive FDA 510(k) clearance?

THE MCP-70-SE SYSTEM received FDA 510(k) clearance on 1985-02-01, under 510(k) number K844180.

Who is the listed applicant for THE MCP-70-SE SYSTEM?

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

What is the FDA product code for THE MCP-70-SE SYSTEM?

The FDA product code for THE MCP-70-SE SYSTEM is KQA.

Related Clinical Trials

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Other records listing Ellis Pharmaceutical Consulting, 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.

K910936EMPTY I.V. CONTAINERK884233QUADROJECT(TM)K852235STERETS INJECTION SWABK832789AFTER LOADING BUCHLER

Related Devices (Code: KQA)

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.

K914784PAPILLION PROCTOSCOPEOldelft Corp. of AmericaK885126PHILIPS RT250 COLLIMATOR (PK8050)Perkins Mfg. Co.K790168COLLIMATOR, BILATERIALCmsi

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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