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FDA 510(k)

BARD PARKER 150CC BELLOWS RESERVOIR

K-Number: K854424 · 1985-11-20

Decision Date1985-11-20
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BARD PARKER 150CC BELLOWS RESERVOIR 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 1985-11-20 under 510(k) number K854424. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD PARKER 150CC BELLOWS RESERVOIR?

BARD PARKER 150CC BELLOWS RESERVOIR is a medical device that received FDA 510(k) clearance on 1985-11-20. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K854424.

When did BARD PARKER 150CC BELLOWS RESERVOIR receive FDA 510(k) clearance?

BARD PARKER 150CC BELLOWS RESERVOIR received FDA 510(k) clearance on 1985-11-20, under 510(k) number K854424.

Who is the listed applicant for BARD PARKER 150CC BELLOWS RESERVOIR?

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 150CC BELLOWS RESERVOIR?

The FDA product code for BARD PARKER 150CC BELLOWS RESERVOIR is GCY.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 devices →

Related Devices (Code: GCY)

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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