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)

DISPOSABLE STYLETTE WITH END CAP

K-Number: K914965 · 1992-05-27

Decision Date1992-05-27
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE STYLETTE WITH END CAP is the device name listed in this FDA 510(k) record. The listed applicant is Pivic Promedco. It received FDA 510(k) clearance on 1992-05-27 under 510(k) number K914965. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE STYLETTE WITH END CAP?

DISPOSABLE STYLETTE WITH END CAP is a medical device that received FDA 510(k) clearance on 1992-05-27. The listed applicant is Pivic Promedco. The 510(k) number is K914965.

When did DISPOSABLE STYLETTE WITH END CAP receive FDA 510(k) clearance?

DISPOSABLE STYLETTE WITH END CAP received FDA 510(k) clearance on 1992-05-27, under 510(k) number K914965.

Who is the listed applicant for DISPOSABLE STYLETTE WITH END CAP?

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

What is the FDA product code for DISPOSABLE STYLETTE WITH END CAP?

The FDA product code for DISPOSABLE STYLETTE WITH END CAP is BSR.

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.

Related Devices (Code: BSR)

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.

↑