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FDA 510(k)

VENOJECT II BLOOD COLLECTION TUBES

K-Number: K900309 · 1990-03-15

ApplicantTerumo Medical Corp.
Decision Date1990-03-15
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VENOJECT II BLOOD COLLECTION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1990-03-15 under 510(k) number K900309. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOJECT II BLOOD COLLECTION TUBES?

VENOJECT II BLOOD COLLECTION TUBES is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is Terumo Medical Corp.. The 510(k) number is K900309.

When did VENOJECT II BLOOD COLLECTION TUBES receive FDA 510(k) clearance?

VENOJECT II BLOOD COLLECTION TUBES received FDA 510(k) clearance on 1990-03-15, under 510(k) number K900309.

Who is the listed applicant for VENOJECT II BLOOD COLLECTION TUBES?

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

What is the FDA product code for VENOJECT II BLOOD COLLECTION TUBES?

The FDA product code for VENOJECT II BLOOD COLLECTION TUBES is JKA.

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Other records listing Terumo Medical Corp. as applicant

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K111606PINNACLE PRECISION ACCESS SYSTEMK111556GLIDECROSS SUPPORT CATHETERK110540TERUMO SUPPORT CATHETERK102008GLIDESHEATHK091329PINNACLE DESTINATION PERIPHERAL GUIDING SHEATHK082997TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER

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Related Devices (Code: JKA)

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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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