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)

MODELS 3987 AND 3988 RESUME LEAD FOR PNS

K-Number: K920567 · 1992-05-20

Decision Date1992-05-20
Product CodeGZF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODELS 3987 AND 3988 RESUME LEAD FOR PNS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1992-05-20 under 510(k) number K920567. The device is classified under product code GZF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS 3987 AND 3988 RESUME LEAD FOR PNS?

MODELS 3987 AND 3988 RESUME LEAD FOR PNS is a medical device that received FDA 510(k) clearance on 1992-05-20. The listed applicant is Medtronic Vascular. The 510(k) number is K920567.

When did MODELS 3987 AND 3988 RESUME LEAD FOR PNS receive FDA 510(k) clearance?

MODELS 3987 AND 3988 RESUME LEAD FOR PNS received FDA 510(k) clearance on 1992-05-20, under 510(k) number K920567.

Who is the listed applicant for MODELS 3987 AND 3988 RESUME LEAD FOR PNS?

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

What is the FDA product code for MODELS 3987 AND 3988 RESUME LEAD FOR PNS?

The FDA product code for MODELS 3987 AND 3988 RESUME LEAD FOR PNS is GZF.

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 Medtronic Vascular 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 474 devices →

Related Devices (Code: GZF)

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.

↑