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FDA 510(k)

VACUUM-ASSISTED BLOOD COLLECTION SYSTEM

K-Number: K905818 · 1991-06-06

ApplicantJtl Medical Corp.
Decision Date1991-06-06
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VACUUM-ASSISTED BLOOD COLLECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Jtl Medical Corp.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K905818. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM-ASSISTED BLOOD COLLECTION SYSTEM?

VACUUM-ASSISTED BLOOD COLLECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Jtl Medical Corp.. The 510(k) number is K905818.

When did VACUUM-ASSISTED BLOOD COLLECTION SYSTEM receive FDA 510(k) clearance?

VACUUM-ASSISTED BLOOD COLLECTION SYSTEM received FDA 510(k) clearance on 1991-06-06, under 510(k) number K905818.

Who is the listed applicant for VACUUM-ASSISTED BLOOD COLLECTION SYSTEM?

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

What is the FDA product code for VACUUM-ASSISTED BLOOD COLLECTION SYSTEM?

The FDA product code for VACUUM-ASSISTED BLOOD COLLECTION SYSTEM is DTN.

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Other records listing Jtl Medical 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.

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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.

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