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FDA 510(k)

ACCESSORY TO 4-24 RECORDER

K-Number: K781129 · 1978-08-31

Decision Date1978-08-31
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACCESSORY TO 4-24 RECORDER 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 1978-08-31 under 510(k) number K781129. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESSORY TO 4-24 RECORDER?

ACCESSORY TO 4-24 RECORDER is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K781129.

When did ACCESSORY TO 4-24 RECORDER receive FDA 510(k) clearance?

ACCESSORY TO 4-24 RECORDER received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781129.

Who is the listed applicant for ACCESSORY TO 4-24 RECORDER?

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 4-24 RECORDER?

The FDA product code for ACCESSORY TO 4-24 RECORDER is GWQ.

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.

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Related Devices (Code: GWQ)

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

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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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