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FDA 510(k)

MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER

K-Number: K940058 · 1994-05-02

Decision Date1994-05-02
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K940058. 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 MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER?

MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Sherwood Medical Co.. The 510(k) number is K940058.

When did MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER receive FDA 510(k) clearance?

MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER received FDA 510(k) clearance on 1994-05-02, under 510(k) number K940058.

Who is the listed applicant for MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER?

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

What is the FDA product code for MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER?

The FDA product code for MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPER 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 Co. 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 191 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

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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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