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FDA 510(k)

BERNARD VESSEL APPROXIMATOR

K-Number: K895683 · 1989-10-24

Decision Date1989-10-24
Product CodeHRQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BERNARD VESSEL APPROXIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1989-10-24 under 510(k) number K895683. The device is classified under product code HRQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BERNARD VESSEL APPROXIMATOR?

BERNARD VESSEL APPROXIMATOR is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Applied Medical Technologies. The 510(k) number is K895683.

When did BERNARD VESSEL APPROXIMATOR receive FDA 510(k) clearance?

BERNARD VESSEL APPROXIMATOR received FDA 510(k) clearance on 1989-10-24, under 510(k) number K895683.

Who is the listed applicant for BERNARD VESSEL APPROXIMATOR?

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

What is the FDA product code for BERNARD VESSEL APPROXIMATOR?

The FDA product code for BERNARD VESSEL APPROXIMATOR is HRQ.

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 Applied Medical Technologies 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 23 devices →

Related Devices (Code: HRQ)

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.

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