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FDA 510(k)

NERVE STIMULATOR MODEL AA 1050

K-Number: K811614 · 1981-06-18

ApplicantAnesthesia Assoc., Inc.
Decision Date1981-06-18
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NERVE STIMULATOR MODEL AA 1050 is the device name listed in this FDA 510(k) record. The listed applicant is Anesthesia Assoc., Inc.. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811614. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NERVE STIMULATOR MODEL AA 1050?

NERVE STIMULATOR MODEL AA 1050 is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Anesthesia Assoc., Inc.. The 510(k) number is K811614.

When did NERVE STIMULATOR MODEL AA 1050 receive FDA 510(k) clearance?

NERVE STIMULATOR MODEL AA 1050 received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811614.

Who is the listed applicant for NERVE STIMULATOR MODEL AA 1050?

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

What is the FDA product code for NERVE STIMULATOR MODEL AA 1050?

The FDA product code for NERVE STIMULATOR MODEL AA 1050 is BXN.

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.

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Other records listing Anesthesia Assoc., 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.

K921926JET VENTILATOR/JETTING DEVICEK833871UNIVERSAL CONTROL ARM

Related Devices (Code: BXN)

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.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (Pty), 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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