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FDA 510(k)

MEDCOMP DISPOSABLE MANIFOLD SYSTEM

K-Number: K863661 · 1986-09-29

ApplicantMedical Components, Inc.
Decision Date1986-09-29
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDCOMP DISPOSABLE MANIFOLD SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Components, Inc.. It received FDA 510(k) clearance on 1986-09-29 under 510(k) number K863661. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCOMP DISPOSABLE MANIFOLD SYSTEM?

MEDCOMP DISPOSABLE MANIFOLD SYSTEM is a medical device that received FDA 510(k) clearance on 1986-09-29. The listed applicant is Medical Components, Inc.. The 510(k) number is K863661.

When did MEDCOMP DISPOSABLE MANIFOLD SYSTEM receive FDA 510(k) clearance?

MEDCOMP DISPOSABLE MANIFOLD SYSTEM received FDA 510(k) clearance on 1986-09-29, under 510(k) number K863661.

Who is the listed applicant for MEDCOMP DISPOSABLE MANIFOLD SYSTEM?

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

What is the FDA product code for MEDCOMP DISPOSABLE MANIFOLD SYSTEM?

The FDA product code for MEDCOMP DISPOSABLE MANIFOLD SYSTEM is DTL.

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Other records listing Medical Components, Inc. as applicant

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Related Devices (Code: DTL)

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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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