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)

BLOOD COLLECTION TUBE, RED

K-Number: K771055 · 1977-06-29

Decision Date1977-06-29
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD COLLECTION TUBE, RED is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-06-29 under 510(k) number K771055. 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 BLOOD COLLECTION TUBE, RED?

BLOOD COLLECTION TUBE, RED is a medical device that received FDA 510(k) clearance on 1977-06-29. The listed applicant is Sherwood Medical Industries. The 510(k) number is K771055.

When did BLOOD COLLECTION TUBE, RED receive FDA 510(k) clearance?

BLOOD COLLECTION TUBE, RED received FDA 510(k) clearance on 1977-06-29, under 510(k) number K771055.

Who is the listed applicant for BLOOD COLLECTION TUBE, RED?

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

What is the FDA product code for BLOOD COLLECTION TUBE, RED?

The FDA product code for BLOOD COLLECTION TUBE, RED 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 Sherwood Medical Industries 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 62 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.

↑