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FDA 510(k)

PARACERVICAL/PUDENDAL TRAYS

K-Number: K896799 · 1990-04-23

Decision Date1990-04-23
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PARACERVICAL/PUDENDAL TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Westmark, Sterile Packing Systems, Inc. (Sps). It received FDA 510(k) clearance on 1990-04-23 under 510(k) number K896799. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARACERVICAL/PUDENDAL TRAYS?

PARACERVICAL/PUDENDAL TRAYS is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is Westmark, Sterile Packing Systems, Inc. (Sps). The 510(k) number is K896799.

When did PARACERVICAL/PUDENDAL TRAYS receive FDA 510(k) clearance?

PARACERVICAL/PUDENDAL TRAYS received FDA 510(k) clearance on 1990-04-23, under 510(k) number K896799.

Who is the listed applicant for PARACERVICAL/PUDENDAL TRAYS?

The FDA 510(k) record lists Westmark, Sterile Packing Systems, Inc. (Sps) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARACERVICAL/PUDENDAL TRAYS?

The FDA product code for PARACERVICAL/PUDENDAL TRAYS is CAZ.

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 Westmark, Sterile Packing Systems, Inc. (Sps) 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 28 devices →

Related Devices (Code: CAZ)

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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