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FDA 510(k)

SAMPLE MANIFOLD HOLDER

K-Number: K860889 · 1986-04-07

ApplicantR. Bell
Decision Date1986-04-07
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAMPLE MANIFOLD HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is R. Bell. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K860889. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAMPLE MANIFOLD HOLDER?

SAMPLE MANIFOLD HOLDER is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is R. Bell. The 510(k) number is K860889.

When did SAMPLE MANIFOLD HOLDER receive FDA 510(k) clearance?

SAMPLE MANIFOLD HOLDER received FDA 510(k) clearance on 1986-04-07, under 510(k) number K860889.

Who is the listed applicant for SAMPLE MANIFOLD HOLDER?

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

What is the FDA product code for SAMPLE MANIFOLD HOLDER?

The FDA product code for SAMPLE MANIFOLD HOLDER is FMG.

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Related Devices (Code: FMG)

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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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