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FDA 510(k)

MORTARA INSTRUMENT, INC. E-SCRIBE

K-Number: K930558 · 1993-04-27

ApplicantMortara Instrument, Inc.
Decision Date1993-04-27
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA INSTRUMENT, INC. E-SCRIBE 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 1993-04-27 under 510(k) number K930558. 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, INC. E-SCRIBE?

MORTARA INSTRUMENT, INC. E-SCRIBE is a medical device that received FDA 510(k) clearance on 1993-04-27. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K930558.

When did MORTARA INSTRUMENT, INC. E-SCRIBE receive FDA 510(k) clearance?

MORTARA INSTRUMENT, INC. E-SCRIBE received FDA 510(k) clearance on 1993-04-27, under 510(k) number K930558.

Who is the listed applicant for MORTARA INSTRUMENT, INC. E-SCRIBE?

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, INC. E-SCRIBE?

The FDA product code for MORTARA INSTRUMENT, INC. E-SCRIBE 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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