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FDA 510(k)

MODEL 808 ADAPTER

K-Number: K792150 · 1979-12-06

ApplicantMalibu Laboratories
Decision Date1979-12-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 808 ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Malibu Laboratories. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792150. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 808 ADAPTER?

MODEL 808 ADAPTER is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Malibu Laboratories. The 510(k) number is K792150.

When did MODEL 808 ADAPTER receive FDA 510(k) clearance?

MODEL 808 ADAPTER received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792150.

Who is the listed applicant for MODEL 808 ADAPTER?

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

What is the FDA product code for MODEL 808 ADAPTER?

The FDA product code for MODEL 808 ADAPTER is GEI.

Related Clinical Trials

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Other records listing Malibu Laboratories 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.

K800022MODEL 807 SUCTION CAUTERY FINGER TIPK791224MALIBU LABS MODEL 800 FINGER TIP CONT

Related Devices (Code: GEI)

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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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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