Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GREINER VACUETTE BLOOD COLLECTION TUBE

K-Number: K971221 · 1997-05-02

Decision Date1997-05-02
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GREINER VACUETTE BLOOD COLLECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Greiner America, Inc.. It received FDA 510(k) clearance on 1997-05-02 under 510(k) number K971221. 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 GREINER VACUETTE BLOOD COLLECTION TUBE?

GREINER VACUETTE BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1997-05-02. The listed applicant is Greiner America, Inc.. The 510(k) number is K971221.

When did GREINER VACUETTE BLOOD COLLECTION TUBE receive FDA 510(k) clearance?

GREINER VACUETTE BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1997-05-02, under 510(k) number K971221.

Who is the listed applicant for GREINER VACUETTE BLOOD COLLECTION TUBE?

The FDA 510(k) record lists Greiner America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREINER VACUETTE BLOOD COLLECTION TUBE?

The FDA product code for GREINER VACUETTE BLOOD COLLECTION TUBE 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.

Other records listing Greiner America, Inc. 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: 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.

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.

↑