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FDA 510(k)

PEDIATRIC EXTEN. SET FOR SECOND-DRUG

K-Number: K830198 · 1983-02-07

ApplicantTravenol Laboratories, S.A.
Decision Date1983-02-07
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC EXTEN. SET FOR SECOND-DRUG 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 1983-02-07 under 510(k) number K830198. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC EXTEN. SET FOR SECOND-DRUG?

PEDIATRIC EXTEN. SET FOR SECOND-DRUG is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K830198.

When did PEDIATRIC EXTEN. SET FOR SECOND-DRUG receive FDA 510(k) clearance?

PEDIATRIC EXTEN. SET FOR SECOND-DRUG received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830198.

Who is the listed applicant for PEDIATRIC EXTEN. SET FOR SECOND-DRUG?

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 PEDIATRIC EXTEN. SET FOR SECOND-DRUG?

The FDA product code for PEDIATRIC EXTEN. SET FOR SECOND-DRUG is FMG.

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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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