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FDA 510(k)

SUCTION KIT

K-Number: K760586 · 1976-11-12

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1976-11-12
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760586. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION KIT?

SUCTION KIT is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760586.

When did SUCTION KIT receive FDA 510(k) clearance?

SUCTION KIT received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760586.

Who is the listed applicant for SUCTION KIT?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION KIT?

The FDA product code for SUCTION KIT is JOL.

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Related Devices (Code: JOL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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