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FDA 510(k)

DIPRIVAN LUER CONNECTOR

K-Number: K935274 · 1994-03-15

ApplicantOhmeda Medical
Decision Date1994-03-15
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIPRIVAN LUER CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1994-03-15 under 510(k) number K935274. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIPRIVAN LUER CONNECTOR?

DIPRIVAN LUER CONNECTOR is a medical device that received FDA 510(k) clearance on 1994-03-15. The listed applicant is Ohmeda Medical. The 510(k) number is K935274.

When did DIPRIVAN LUER CONNECTOR receive FDA 510(k) clearance?

DIPRIVAN LUER CONNECTOR received FDA 510(k) clearance on 1994-03-15, under 510(k) number K935274.

Who is the listed applicant for DIPRIVAN LUER CONNECTOR?

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

What is the FDA product code for DIPRIVAN LUER CONNECTOR?

The FDA product code for DIPRIVAN LUER CONNECTOR is LHI.

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Related Devices (Code: LHI)

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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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