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FDA 510(k)

VACUUM TUBES, PEDIATRIC SIZES (J-VAC)

K-Number: K760019 · 1976-07-20

ApplicantJelco Laboratories
Decision Date1976-07-20
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUUM TUBES, PEDIATRIC SIZES (J-VAC) is the device name listed in this FDA 510(k) record. The listed applicant is Jelco Laboratories. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760019. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM TUBES, PEDIATRIC SIZES (J-VAC)?

VACUUM TUBES, PEDIATRIC SIZES (J-VAC) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Jelco Laboratories. The 510(k) number is K760019.

When did VACUUM TUBES, PEDIATRIC SIZES (J-VAC) receive FDA 510(k) clearance?

VACUUM TUBES, PEDIATRIC SIZES (J-VAC) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760019.

Who is the listed applicant for VACUUM TUBES, PEDIATRIC SIZES (J-VAC)?

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

What is the FDA product code for VACUUM TUBES, PEDIATRIC SIZES (J-VAC)?

The FDA product code for VACUUM TUBES, PEDIATRIC SIZES (J-VAC) is GIM.

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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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