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FDA 510(k)

PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2

K-Number: K945273 · 1994-12-14

Decision Date1994-12-14
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2 is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tec Containers, Inc.. It received FDA 510(k) clearance on 1994-12-14 under 510(k) number K945273. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2?

PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2 is a medical device that received FDA 510(k) clearance on 1994-12-14. The listed applicant is Pro-Tec Containers, Inc.. The 510(k) number is K945273.

When did PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2 receive FDA 510(k) clearance?

PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2 received FDA 510(k) clearance on 1994-12-14, under 510(k) number K945273.

Who is the listed applicant for PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2?

The FDA 510(k) record lists Pro-Tec Containers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2?

The FDA product code for PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2 is FMI.

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 Pro-Tec Containers, 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.

Related Devices (Code: FMI)

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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