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FDA 510(k)

MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST

K-Number: K925591 · 1993-09-16

ApplicantMerit Medical Systems, Inc.
Decision Date1993-09-16
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-09-16 under 510(k) number K925591. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST?

MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K925591.

When did MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST receive FDA 510(k) clearance?

MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST received FDA 510(k) clearance on 1993-09-16, under 510(k) number K925591.

Who is the listed applicant for MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST?

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

What is the FDA product code for MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST?

The FDA product code for MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST is BZR.

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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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