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FDA 510(k)

DORROS-SPRING PRESSURIZER

K-Number: K812304 · 1981-10-13

ApplicantCardiovascular Diagnostic Services
Decision Date1981-10-13
Product CodeMAV
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DORROS-SPRING PRESSURIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cardiovascular Diagnostic Services. It received FDA 510(k) clearance on 1981-10-13 under 510(k) number K812304. The device is classified under product code MAV. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORROS-SPRING PRESSURIZER?

DORROS-SPRING PRESSURIZER is a medical device that received FDA 510(k) clearance on 1981-10-13. The listed applicant is Cardiovascular Diagnostic Services. The 510(k) number is K812304.

When did DORROS-SPRING PRESSURIZER receive FDA 510(k) clearance?

DORROS-SPRING PRESSURIZER received FDA 510(k) clearance on 1981-10-13, under 510(k) number K812304.

Who is the listed applicant for DORROS-SPRING PRESSURIZER?

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

What is the FDA product code for DORROS-SPRING PRESSURIZER?

The FDA product code for DORROS-SPRING PRESSURIZER is MAV.

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Other records listing Cardiovascular Diagnostic Services 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.

K955843TAS PTONEK933092TAS ANALYZERK904325COAG-1 PT-NC TEST CARDK903019MODIFIED COAG-1 PT TEST CARDK891015COAG-1 APTT TEST CARDK882456COAG-I PT TEST CARD

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Related Devices (Code: MAV)

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.

K260035Digital Indeflator INFLANTEUAB TelemedicinaK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)Medtronic VascularK162272Fluent inflation deviceVascular Solutions, Inc.K153038Everest 20 Disposable Inflation Device, Everest 20 Survival Kit, Everest 30 Disposable Inflation Device, Everest 30 Survival KitMedtronic, Inc.K153672basixTOUCH40 Inflation SyringeMerit Medical Systems, Inc.K130566BASIXTOUCHMerit Medical Systems, 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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