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FDA 510(k)

BVR CONTRA-ANGLE HANDPIECE

K-Number: K934571 · 1994-08-01

Decision Date1994-08-01
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BVR CONTRA-ANGLE HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Bvr Aero Precision Corp.. It received FDA 510(k) clearance on 1994-08-01 under 510(k) number K934571. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BVR CONTRA-ANGLE HANDPIECE?

BVR CONTRA-ANGLE HANDPIECE is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Bvr Aero Precision Corp.. The 510(k) number is K934571.

When did BVR CONTRA-ANGLE HANDPIECE receive FDA 510(k) clearance?

BVR CONTRA-ANGLE HANDPIECE received FDA 510(k) clearance on 1994-08-01, under 510(k) number K934571.

Who is the listed applicant for BVR CONTRA-ANGLE HANDPIECE?

The FDA 510(k) record lists Bvr Aero Precision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BVR CONTRA-ANGLE HANDPIECE?

The FDA product code for BVR CONTRA-ANGLE HANDPIECE is EGS.

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 Bvr Aero Precision 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.

Related Devices (Code: EGS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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