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FDA 510(k)

PIPERACILLIN/TAZOBACTAM 4

K-Number: K964203 · 1996-12-18

ApplicantAb Biodisk
Decision Date1996-12-18
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PIPERACILLIN/TAZOBACTAM 4 is the device name listed in this FDA 510(k) record. The listed applicant is Ab Biodisk. It received FDA 510(k) clearance on 1996-12-18 under 510(k) number K964203. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIPERACILLIN/TAZOBACTAM 4?

PIPERACILLIN/TAZOBACTAM 4 is a medical device that received FDA 510(k) clearance on 1996-12-18. The listed applicant is Ab Biodisk. The 510(k) number is K964203.

When did PIPERACILLIN/TAZOBACTAM 4 receive FDA 510(k) clearance?

PIPERACILLIN/TAZOBACTAM 4 received FDA 510(k) clearance on 1996-12-18, under 510(k) number K964203.

Who is the listed applicant for PIPERACILLIN/TAZOBACTAM 4?

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

What is the FDA product code for PIPERACILLIN/TAZOBACTAM 4?

The FDA product code for PIPERACILLIN/TAZOBACTAM 4 is JWY.

Related Clinical Trials

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Other records listing Ab Biodisk 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.

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Related Devices (Code: JWY)

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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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