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FDA 510(k)

ONE-WAY AIR VALVE

K-Number: K840253 · 1984-04-05

ApplicantDelta Medical Industries
Decision Date1984-04-05
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ONE-WAY AIR VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K840253. The device is classified under product code BYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE-WAY AIR VALVE?

ONE-WAY AIR VALVE is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Delta Medical Industries. The 510(k) number is K840253.

When did ONE-WAY AIR VALVE receive FDA 510(k) clearance?

ONE-WAY AIR VALVE received FDA 510(k) clearance on 1984-04-05, under 510(k) number K840253.

Who is the listed applicant for ONE-WAY AIR VALVE?

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

What is the FDA product code for ONE-WAY AIR VALVE?

The FDA product code for ONE-WAY AIR VALVE is BYZ.

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Other records listing Delta Medical Industries as applicant

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.

K833884ISOTEC DISPOS. PRESSURE TRANSDUCERK832470INFUSION PUMPK830389ACCU-RYNGE PUMP SP-250K831750PM-3K822761DELIVERY TUBE SET #2226K820912PMS-2 PRESSURE MONITOR SEPARATOR

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Related Devices (Code: BYZ)

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.

K925412ELECTROMEDICS TISSUE TRAP/ #TT280Electromedics, Inc.K913643MUCOUS SPECIMEN TRAPMedical Device Inspection Co., Inc.K902883TISSUE/POLYP TRAP SYSTEMTriton Technology, Inc.K841409BUSH NECK W/PLUGWarne Surgical Products, Ltd.K834467SPECIMEN TRAPMicrovasiveK822557SPECIMEN ADAPTORBemis Health Care

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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