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FDA 510(k)

FILTER, VACUUM LINE LINEGUARD

K-Number: K760420 · 1976-08-23

ApplicantDiemolding Corp.
Decision Date1976-08-23
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FILTER, VACUUM LINE LINEGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Diemolding Corp.. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760420. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER, VACUUM LINE LINEGUARD?

FILTER, VACUUM LINE LINEGUARD is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Diemolding Corp.. The 510(k) number is K760420.

When did FILTER, VACUUM LINE LINEGUARD receive FDA 510(k) clearance?

FILTER, VACUUM LINE LINEGUARD received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760420.

Who is the listed applicant for FILTER, VACUUM LINE LINEGUARD?

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 FILTER, VACUUM LINE LINEGUARD?

The FDA product code for FILTER, VACUUM LINE LINEGUARD is KPQ.

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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: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, LLC

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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