EXTENSION SETS
K-Number: K864692 · 1986-12-18
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Device Summary
Frequently Asked Questions
What is the EXTENSION SETS?
EXTENSION SETS is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Salt Creek Medical Technologies. The 510(k) number is K864692.
When did EXTENSION SETS receive FDA 510(k) clearance?
EXTENSION SETS received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864692.
Who is the listed applicant for EXTENSION SETS?
The FDA 510(k) record lists Salt Creek Medical Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXTENSION SETS?
The FDA product code for EXTENSION SETS is FPK.
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 Salt Creek Medical Technologies 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: FPK)
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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