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FDA 510(k)

PACEVIEW

K-Number: K915627 · 1992-03-27

ApplicantMicromedical Industries, Ltd.
Decision Date1992-03-27
Product CodeKRB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PACEVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Micromedical Industries, Ltd.. It received FDA 510(k) clearance on 1992-03-27 under 510(k) number K915627. The device is classified under product code KRB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACEVIEW?

PACEVIEW is a medical device that received FDA 510(k) clearance on 1992-03-27. The listed applicant is Micromedical Industries, Ltd.. The 510(k) number is K915627.

When did PACEVIEW receive FDA 510(k) clearance?

PACEVIEW received FDA 510(k) clearance on 1992-03-27, under 510(k) number K915627.

Who is the listed applicant for PACEVIEW?

The FDA 510(k) record lists Micromedical Industries, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PACEVIEW?

The FDA product code for PACEVIEW is KRB.

Related Clinical Trials

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.

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Other records listing Micromedical Industries, Ltd. 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.

K013311MODIFICATION TO: POCKETVIEW ECG SOFTWAREK012540BLY-501 ADAPTORK990266MICROMEDICAL 12 LEAD SIMULTANEOUS CABLEK922528CMS SYSTEMK915624MODIFIED BIOLOG

Related Devices (Code: KRB)

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.

K171620PiCCO CatheterPulsion Medical Systems SEK100739VOLUMEVIEW SYSTEM, MODELS VLV520FT6R, VLV520FT8R, VLV520FT6R5Edwards Lifesciences, LLCK072364PULSION PULSIOCATH THERMODILUTION CATHETERS & ACCESSORIESPulsion Medical Systems AGK020587PULSION PULSIOCATH PICCO MONITORING KIT, INJECTATE SENSOR TEMPERATURE HOUSING PV 4046Pulsion Medical Systems AGK991886PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSORPulsion Medical Systems, Inc.K936182CRITIKIT PLUS IN LINE ROOM/ICE TEMPERATURE INJECTATE KITOhmeda Medical

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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