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FDA 510(k)

ACCESSORY TO ECG ANALYSIS SYS.

K-Number: K781130 · 1978-08-23

Decision Date1978-08-23
Product CodeOMC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACCESSORY TO ECG ANALYSIS SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1978-08-23 under 510(k) number K781130. The device is classified under product code OMC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESSORY TO ECG ANALYSIS SYS.?

ACCESSORY TO ECG ANALYSIS SYS. is a medical device that received FDA 510(k) clearance on 1978-08-23. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K781130.

When did ACCESSORY TO ECG ANALYSIS SYS. receive FDA 510(k) clearance?

ACCESSORY TO ECG ANALYSIS SYS. received FDA 510(k) clearance on 1978-08-23, under 510(k) number K781130.

Who is the listed applicant for ACCESSORY TO ECG ANALYSIS SYS.?

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

What is the FDA product code for ACCESSORY TO ECG ANALYSIS SYS.?

The FDA product code for ACCESSORY TO ECG ANALYSIS SYS. is OMC.

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.

Other records listing Oxford Medilog, 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.

View all 48 devices →

Related Devices (Code: OMC)

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.

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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