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)

TAPE, VASCULAR, 1/4 DACRON

K-Number: K760087 · 1976-07-20

Decision Date1976-07-20
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAPE, VASCULAR, 1/4 DACRON is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760087. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAPE, VASCULAR, 1/4 DACRON?

TAPE, VASCULAR, 1/4 DACRON is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K760087.

When did TAPE, VASCULAR, 1/4 DACRON receive FDA 510(k) clearance?

TAPE, VASCULAR, 1/4 DACRON received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760087.

Who is the listed applicant for TAPE, VASCULAR, 1/4 DACRON?

The FDA 510(k) record lists Meadox Medicals, Div. Boston Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAPE, VASCULAR, 1/4 DACRON?

The FDA product code for TAPE, VASCULAR, 1/4 DACRON is DWS.

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 Meadox Medicals, Div. Boston Scientific Corp. 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 53 devices →

Related Devices (Code: DWS)

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.

↑