PILOT TUBE REPAIR KIT
K-Number: K973755 · 1997-12-17
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Device Summary
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.
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
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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