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FDA 510(k)

MEDILOG MPA-S

K-Number: K961638 · 1997-01-17

ApplicantOxford Instruments Medical Systems
Decision Date1997-01-17
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDILOG MPA-S is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Instruments Medical Systems. It received FDA 510(k) clearance on 1997-01-17 under 510(k) number K961638. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILOG MPA-S?

MEDILOG MPA-S is a medical device that received FDA 510(k) clearance on 1997-01-17. The listed applicant is Oxford Instruments Medical Systems. The 510(k) number is K961638.

When did MEDILOG MPA-S receive FDA 510(k) clearance?

MEDILOG MPA-S received FDA 510(k) clearance on 1997-01-17, under 510(k) number K961638.

Who is the listed applicant for MEDILOG MPA-S?

The FDA 510(k) record lists Oxford Instruments Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDILOG MPA-S?

The FDA product code for MEDILOG MPA-S is OLV.

Related Clinical Trials

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Other records listing Oxford Instruments Medical Systems 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.

K992607SONICAID SYSTEM 8002K984052SYNERGY IOM SYSTEMK970902MEDILOG FD4K943862SONICAID MODEL MR-63 AMBULATORY ECG RECORDER

Related Devices (Code: OLV)

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.

K261747Report StudioBeacon Biosignals, Inc.K260585Noxturnal WebNox Medical EhfK242447Falcon HSTCompumedics LimitedK241288Noxturnal WebNox Medical EhfK240700HomeSleepTest (HST, HST REM+)Somnomedics GmbHK213007Cerebra Sleep SystemCerebra Medical , Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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