FDA 510(k)

FASCICULATED BOAT ROD

K-Number: K863239 · 1986-12-24

Decision Date1986-12-24

Product Code

DecisionSubstantially Equivalent

Device Summary

FASCICULATED BOAT ROD is the device name listed in this FDA 510(k) record. The listed applicant is The Deca Co.. It received FDA 510(k) clearance on 1986-12-24 under 510(k) number K863239. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASCICULATED BOAT ROD?

FASCICULATED BOAT ROD is a medical device that received FDA 510(k) clearance on 1986-12-24. The listed applicant is The Deca Co.. The 510(k) number is K863239.

When did FASCICULATED BOAT ROD receive FDA 510(k) clearance?

FASCICULATED BOAT ROD received FDA 510(k) clearance on 1986-12-24, under 510(k) number K863239.

Who is the listed applicant for FASCICULATED BOAT ROD?

The FDA 510(k) record lists The Deca Co. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing The Deca Co. as applicant

K870041FLEXIBLE FASCICULATED BONE PLATE K870040INTRAMEDULLARY NAIL K863215FASCICULATED I ROD K863271FASCICULATED S ROD K861183INTRAMEDULLARY ROD K854227FASCILULATED NAIL

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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.