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FDA 510(k)

PIPERACILIN TAZOBACTAM 4 UG

K-Number: K953223 · 1995-08-15

ApplicantAb Biodisk
Decision Date1995-08-15
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PIPERACILIN TAZOBACTAM 4 UG is the device name listed in this FDA 510(k) record. The listed applicant is Ab Biodisk. It received FDA 510(k) clearance on 1995-08-15 under 510(k) number K953223. 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 PIPERACILIN TAZOBACTAM 4 UG?

PIPERACILIN TAZOBACTAM 4 UG is a medical device that received FDA 510(k) clearance on 1995-08-15. The listed applicant is Ab Biodisk. The 510(k) number is K953223.

When did PIPERACILIN TAZOBACTAM 4 UG receive FDA 510(k) clearance?

PIPERACILIN TAZOBACTAM 4 UG received FDA 510(k) clearance on 1995-08-15, under 510(k) number K953223.

Who is the listed applicant for PIPERACILIN TAZOBACTAM 4 UG?

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 PIPERACILIN TAZOBACTAM 4 UG?

The FDA product code for PIPERACILIN TAZOBACTAM 4 UG is JWY.

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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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