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FDA 510(k)

MORTARA INSTRUMENT ST CENTRAL STATION

K-Number: K922927 · 1992-11-10

ApplicantMortara Instrument, Inc.
Decision Date1992-11-10
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA INSTRUMENT ST CENTRAL STATION is the device name listed in this FDA 510(k) record. The listed applicant is Mortara Instrument, Inc.. It received FDA 510(k) clearance on 1992-11-10 under 510(k) number K922927. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORTARA INSTRUMENT ST CENTRAL STATION?

MORTARA INSTRUMENT ST CENTRAL STATION is a medical device that received FDA 510(k) clearance on 1992-11-10. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K922927.

When did MORTARA INSTRUMENT ST CENTRAL STATION receive FDA 510(k) clearance?

MORTARA INSTRUMENT ST CENTRAL STATION received FDA 510(k) clearance on 1992-11-10, under 510(k) number K922927.

Who is the listed applicant for MORTARA INSTRUMENT ST CENTRAL STATION?

The FDA 510(k) record lists Mortara Instrument, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MORTARA INSTRUMENT ST CENTRAL STATION?

The FDA product code for MORTARA INSTRUMENT ST CENTRAL STATION is DPS.

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Other records listing Mortara Instrument, Inc. 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.

K182297Surveyor S2K173765Surveyor Patient MonitorK161517Mortara Surveyor Patient MonitorK161465CardioConfirmK160685Surveyor S4 Mobile MonitorK152626H3+ Holter Recorder

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Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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