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FDA 510(k)

SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV

K-Number: K974374 · 1998-01-02

ApplicantOhmeda Medical
Decision Date1998-01-02
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1998-01-02 under 510(k) number K974374. 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 SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV?

SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV is a medical device that received FDA 510(k) clearance on 1998-01-02. The listed applicant is Ohmeda Medical. The 510(k) number is K974374.

When did SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV receive FDA 510(k) clearance?

SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV received FDA 510(k) clearance on 1998-01-02, under 510(k) number K974374.

Who is the listed applicant for SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV?

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

What is the FDA product code for SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV?

The FDA product code for SAFE NEEDLE DIRECT BLOOD TRANSFER DEVICE, MODEL TA-STV is 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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