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FDA 510(k)

SURGICAL CONNECTING TUBES

K-Number: K883473 · 1988-08-25

Decision Date1988-08-25
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL CONNECTING TUBES 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 1988-08-25 under 510(k) number K883473. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL CONNECTING TUBES?

SURGICAL CONNECTING TUBES is a medical device that received FDA 510(k) clearance on 1988-08-25. The listed applicant is Westmark, Sterile Packing Systems, Inc. (Sps). The 510(k) number is K883473.

When did SURGICAL CONNECTING TUBES receive FDA 510(k) clearance?

SURGICAL CONNECTING TUBES received FDA 510(k) clearance on 1988-08-25, under 510(k) number K883473.

Who is the listed applicant for SURGICAL CONNECTING TUBES?

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 SURGICAL CONNECTING TUBES?

The FDA product code for SURGICAL CONNECTING TUBES is GAZ.

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: GAZ)

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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