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FDA 510(k)

O2 CONNECTOR

K-Number: K780750 · 1978-07-27

ApplicantDiemolding Corp.
Decision Date1978-07-27
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

O2 CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Diemolding Corp.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K780750. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the O2 CONNECTOR?

O2 CONNECTOR is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Diemolding Corp.. The 510(k) number is K780750.

When did O2 CONNECTOR receive FDA 510(k) clearance?

O2 CONNECTOR received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780750.

Who is the listed applicant for O2 CONNECTOR?

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

What is the FDA product code for O2 CONNECTOR?

The FDA product code for O2 CONNECTOR is CAN.

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Other records listing Diemolding Corp. 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.

K962749THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORTK961455MEDSHIELD/AEROCHAMBERK902713ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANSK902114CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITORK900754RESPIREX 2K893791BREATHING MOUTHPIECE

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Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., 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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