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FDA 510(k)

BVN

K-Number: K800695 · 1980-05-02

ApplicantDonald J. Mangus, M.D.
Decision Date1980-05-02
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BVN is the device name listed in this FDA 510(k) record. The listed applicant is Donald J. Mangus, M.D.. It received FDA 510(k) clearance on 1980-05-02 under 510(k) number K800695. The device is classified under product code ITG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BVN?

BVN is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Donald J. Mangus, M.D.. The 510(k) number is K800695.

When did BVN receive FDA 510(k) clearance?

BVN received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800695.

Who is the listed applicant for BVN?

The FDA 510(k) record lists Donald J. Mangus, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BVN?

The FDA product code for BVN is ITG.

Related Devices (Code: ITG)

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.

K873111CONFORMA(TM) PLASTER BANDAGESThe Kendal Co.K862115DEKNA BAND KITDeknatel, Inc.K842573T.P.G. CAST TAPEThe Poly Group, Inc.K840416HEXCELITEHexcel MedicalK833732NON WETTING UNDERCAST PADDINGAmerican Medical Disposable, Inc.K832992SOFFBAN ORTHOPEDIC PADDINGSmith & Nephew, Inc.

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.

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