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FDA 510(k)

BARD PARKER THORACIC VENT

K-Number: K854634 · 1985-12-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1985-12-27
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD PARKER THORACIC VENT is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1985-12-27 under 510(k) number K854634. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD PARKER THORACIC VENT?

BARD PARKER THORACIC VENT is a medical device that received FDA 510(k) clearance on 1985-12-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K854634.

When did BARD PARKER THORACIC VENT receive FDA 510(k) clearance?

BARD PARKER THORACIC VENT received FDA 510(k) clearance on 1985-12-27, under 510(k) number K854634.

Who is the listed applicant for BARD PARKER THORACIC VENT?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD PARKER THORACIC VENT?

The FDA product code for BARD PARKER THORACIC VENT is KDQ.

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Related Devices (Code: KDQ)

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.

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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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