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)

B-D GUARDIAN NESTABLE SHARPS COLLECTORS

K-Number: K943134 · 1994-11-07

Decision Date1994-11-07
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

B-D GUARDIAN NESTABLE SHARPS COLLECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Med-Safe Systems, Inc.. It received FDA 510(k) clearance on 1994-11-07 under 510(k) number K943134. 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 B-D GUARDIAN NESTABLE SHARPS COLLECTORS?

B-D GUARDIAN NESTABLE SHARPS COLLECTORS is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Med-Safe Systems, Inc.. The 510(k) number is K943134.

When did B-D GUARDIAN NESTABLE SHARPS COLLECTORS receive FDA 510(k) clearance?

B-D GUARDIAN NESTABLE SHARPS COLLECTORS received FDA 510(k) clearance on 1994-11-07, under 510(k) number K943134.

Who is the listed applicant for B-D GUARDIAN NESTABLE SHARPS COLLECTORS?

The FDA 510(k) record lists Med-Safe Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B-D GUARDIAN NESTABLE SHARPS COLLECTORS?

The FDA product code for B-D GUARDIAN NESTABLE SHARPS COLLECTORS 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 Med-Safe Systems, 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 8 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑