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FDA 510(k)

VACUUM TUBES, STERILE (J-VAC)

K-Number: K760018 · 1976-07-20

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

Device Summary

VACUUM TUBES, STERILE (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 K760018. 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, STERILE (J-VAC)?

VACUUM TUBES, STERILE (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 K760018.

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

VACUUM TUBES, STERILE (J-VAC) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760018.

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

The FDA product code for VACUUM TUBES, STERILE (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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