FDA 510(k)

EXEL VACUUM BLOOD COLLECTING SYSTEM

K-Number: K861152 · 1986-05-06

Decision Date1986-05-06

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

EXEL VACUUM BLOOD COLLECTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Exel Intl.. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K861152. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXEL VACUUM BLOOD COLLECTING SYSTEM?

EXEL VACUUM BLOOD COLLECTING SYSTEM is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Exel Intl.. The 510(k) number is K861152.

When did EXEL VACUUM BLOOD COLLECTING SYSTEM receive FDA 510(k) clearance?

EXEL VACUUM BLOOD COLLECTING SYSTEM received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861152.

Who is the listed applicant for EXEL VACUUM BLOOD COLLECTING SYSTEM?

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

What is the FDA product code for EXEL VACUUM BLOOD COLLECTING SYSTEM?

The FDA product code for EXEL VACUUM BLOOD COLLECTING SYSTEM is FMI.

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Other records listing Exel Intl. as applicant

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Related Devices (Code: FMI)

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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.