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FDA 510(k)

MONITOR/MINI SCOPE

K-Number: K781679 · 1978-12-12

ApplicantIpco Corp.
Decision Date1978-12-12
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR/MINI SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1978-12-12 under 510(k) number K781679. 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 MONITOR/MINI SCOPE?

MONITOR/MINI SCOPE is a medical device that received FDA 510(k) clearance on 1978-12-12. The listed applicant is Ipco Corp.. The 510(k) number is K781679.

When did MONITOR/MINI SCOPE receive FDA 510(k) clearance?

MONITOR/MINI SCOPE received FDA 510(k) clearance on 1978-12-12, under 510(k) number K781679.

Who is the listed applicant for MONITOR/MINI SCOPE?

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

What is the FDA product code for MONITOR/MINI SCOPE?

The FDA product code for MONITOR/MINI SCOPE is DPS.

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Other records listing Ipco 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.

K871270PERFORM DENTURE BASE RESINK850666STROBEX ULTRON ELECTROSURGE-DENTAL UNITK850906TACTILE PLUS DENTAL ELEVATORSK842836SAFE & SOFT MINI PADS & MAXI PADSK842837SAFE & SOFT MAXI SHILEDSK842838SAFE & SOFT PANTY SHIELDS

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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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