KRONNER LOW PROFILE SCOPE HOLDER
K-Number: K973543 · 1998-01-12
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Device Summary
Frequently Asked Questions
What is the KRONNER LOW PROFILE SCOPE HOLDER?
KRONNER LOW PROFILE SCOPE HOLDER is a medical device that received FDA 510(k) clearance on 1998-01-12. The listed applicant is Kronner Prototypes, Inc.. The 510(k) number is K973543.
When did KRONNER LOW PROFILE SCOPE HOLDER receive FDA 510(k) clearance?
KRONNER LOW PROFILE SCOPE HOLDER received FDA 510(k) clearance on 1998-01-12, under 510(k) number K973543.
Who is the listed applicant for KRONNER LOW PROFILE SCOPE HOLDER?
The FDA 510(k) record lists Kronner Prototypes, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KRONNER LOW PROFILE SCOPE HOLDER?
The FDA product code for KRONNER LOW PROFILE SCOPE HOLDER is GCJ.
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 Kronner Prototypes, 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: GCJ)
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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