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FDA 510(k)

CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186

K-Number: K860700 · 1986-04-07

ApplicantTravenol Laboratories, S.A.
Decision Date1986-04-07
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K860700. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186?

CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186 is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K860700.

When did CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186 receive FDA 510(k) clearance?

CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186 received FDA 510(k) clearance on 1986-04-07, under 510(k) number K860700.

Who is the listed applicant for CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186?

The FDA product code for CAPD DISCONNECT SYSTEM 5C4182, 5C4183, 5C4186 is KDJ.

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Other records listing Travenol Laboratories, S.A. as applicant

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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.

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