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FDA 510(k)

SYRINGE FOR BLOOD SAMPLING

K-Number: K803182 · 1981-01-16

ApplicantThe University of Chicago
Decision Date1981-01-16
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYRINGE FOR BLOOD SAMPLING is the device name listed in this FDA 510(k) record. The listed applicant is The University of Chicago. It received FDA 510(k) clearance on 1981-01-16 under 510(k) number K803182. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGE FOR BLOOD SAMPLING?

SYRINGE FOR BLOOD SAMPLING is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is The University of Chicago. The 510(k) number is K803182.

When did SYRINGE FOR BLOOD SAMPLING receive FDA 510(k) clearance?

SYRINGE FOR BLOOD SAMPLING received FDA 510(k) clearance on 1981-01-16, under 510(k) number K803182.

Who is the listed applicant for SYRINGE FOR BLOOD SAMPLING?

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

What is the FDA product code for SYRINGE FOR BLOOD SAMPLING?

The FDA product code for SYRINGE FOR BLOOD SAMPLING is GIM.

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.

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Other records listing The University of Chicago 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.

K803302PREHEPARINZED SYRINGE

Related Devices (Code: GIM)

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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