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FDA 510(k)

PILOT TUBE REPAIR KIT

K-Number: K973755 · 1997-12-17

Decision Date1997-12-17
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PILOT TUBE REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K973755. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILOT TUBE REPAIR KIT?

PILOT TUBE REPAIR KIT is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K973755.

When did PILOT TUBE REPAIR KIT receive FDA 510(k) clearance?

PILOT TUBE REPAIR KIT received FDA 510(k) clearance on 1997-12-17, under 510(k) number K973755.

Who is the listed applicant for PILOT TUBE REPAIR KIT?

The FDA 510(k) record lists Instrumentation Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PILOT TUBE REPAIR KIT?

The FDA product code for PILOT TUBE REPAIR KIT is BSK.

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 Instrumentation Industries, Inc. 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 45 devices →

Related Devices (Code: BSK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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