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-WRAP

K-Number: K863777 · 1986-10-24

ApplicantBdf Plaza
Decision Date1986-10-24
Product Code
DecisionSubstantially Equivalent

Device Summary

B-WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Bdf Plaza. It received FDA 510(k) clearance on 1986-10-24 under 510(k) number K863777. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-WRAP?

B-WRAP is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Bdf Plaza. The 510(k) number is K863777.

When did B-WRAP receive FDA 510(k) clearance?

B-WRAP received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863777.

Who is the listed applicant for B-WRAP?

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

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.

↑