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FDA 510(k)

BLOOD GAS SAFETY SYRINGE

K-Number: K895171 · 1989-11-07

Decision Date1989-11-07
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Medical. It received FDA 510(k) clearance on 1989-11-07 under 510(k) number K895171. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS SAFETY SYRINGE?

BLOOD GAS SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 1989-11-07. The listed applicant is Kronner Medical. The 510(k) number is K895171.

When did BLOOD GAS SAFETY SYRINGE receive FDA 510(k) clearance?

BLOOD GAS SAFETY SYRINGE received FDA 510(k) clearance on 1989-11-07, under 510(k) number K895171.

Who is the listed applicant for BLOOD GAS SAFETY SYRINGE?

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

What is the FDA product code for BLOOD GAS SAFETY SYRINGE?

The FDA product code for BLOOD GAS SAFETY SYRINGE is CBT.

Related Clinical Trials

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.

Other records listing Kronner Medical 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.

View all 7 devices →

Related Devices (Code: CBT)

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.

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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