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FDA 510(k)

PBC IV SET VENTED

K-Number: K834254 · 1984-02-27

Decision Date1984-02-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PBC IV SET VENTED is the device name listed in this FDA 510(k) record. The listed applicant is Philadelphia Biologics Center. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K834254. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PBC IV SET VENTED?

PBC IV SET VENTED is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Philadelphia Biologics Center. The 510(k) number is K834254.

When did PBC IV SET VENTED receive FDA 510(k) clearance?

PBC IV SET VENTED received FDA 510(k) clearance on 1984-02-27, under 510(k) number K834254.

Who is the listed applicant for PBC IV SET VENTED?

The FDA 510(k) record lists Philadelphia Biologics Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PBC IV SET VENTED?

The FDA product code for PBC IV SET VENTED is FPA.

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 Philadelphia Biologics Center 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 11 devices →

Related Devices (Code: FPA)

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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