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FDA 510(k)

VIAL SYRINGE PUMPS, SE200, SE200B & SE400

K-Number: K852073 · 1985-06-07

ApplicantHospal Medical Corp.
Decision Date1985-06-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIAL SYRINGE PUMPS, SE200, SE200B & SE400 is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1985-06-07 under 510(k) number K852073. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIAL SYRINGE PUMPS, SE200, SE200B & SE400?

VIAL SYRINGE PUMPS, SE200, SE200B & SE400 is a medical device that received FDA 510(k) clearance on 1985-06-07. The listed applicant is Hospal Medical Corp.. The 510(k) number is K852073.

When did VIAL SYRINGE PUMPS, SE200, SE200B & SE400 receive FDA 510(k) clearance?

VIAL SYRINGE PUMPS, SE200, SE200B & SE400 received FDA 510(k) clearance on 1985-06-07, under 510(k) number K852073.

Who is the listed applicant for VIAL SYRINGE PUMPS, SE200, SE200B & SE400?

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

What is the FDA product code for VIAL SYRINGE PUMPS, SE200, SE200B & SE400?

The FDA product code for VIAL SYRINGE PUMPS, SE200, SE200B & SE400 is FRN.

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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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