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FDA 510(k)

MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT

K-Number: K925263 · 1993-02-02

ApplicantMerit Medical Systems, Inc.
Decision Date1993-02-02
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT 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 1993-02-02 under 510(k) number K925263. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT?

MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT is a medical device that received FDA 510(k) clearance on 1993-02-02. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K925263.

When did MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT receive FDA 510(k) clearance?

MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT received FDA 510(k) clearance on 1993-02-02, under 510(k) number K925263.

Who is the listed applicant for MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT?

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 CONNECTORS & AIRWAY EXT?

The FDA product code for MERIDIAN MEDICAL SYSTEMS CONNECTORS & AIRWAY EXT is BZA.

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Related Devices (Code: BZA)

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, Inc.

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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