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FDA 510(k)

MOBIL-AID AUTOMATIC EXPOSURE CONTROL

K-Number: K813128 · 1981-12-03

ApplicantAdvanced Instrument Development, Inc.
Decision Date1981-12-03
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBIL-AID AUTOMATIC EXPOSURE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instrument Development, Inc.. It received FDA 510(k) clearance on 1981-12-03 under 510(k) number K813128. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBIL-AID AUTOMATIC EXPOSURE CONTROL?

MOBIL-AID AUTOMATIC EXPOSURE CONTROL is a medical device that received FDA 510(k) clearance on 1981-12-03. The listed applicant is Advanced Instrument Development, Inc.. The 510(k) number is K813128.

When did MOBIL-AID AUTOMATIC EXPOSURE CONTROL receive FDA 510(k) clearance?

MOBIL-AID AUTOMATIC EXPOSURE CONTROL received FDA 510(k) clearance on 1981-12-03, under 510(k) number K813128.

Who is the listed applicant for MOBIL-AID AUTOMATIC EXPOSURE CONTROL?

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

What is the FDA product code for MOBIL-AID AUTOMATIC EXPOSURE CONTROL?

The FDA product code for MOBIL-AID AUTOMATIC EXPOSURE CONTROL is IZL.

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 Advanced Instrument Development, 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.

K974863IMIX DIGITAL THORAX SYSTEMK872445POWER-AID INDEPENDENT X-RAY POWER SOURCEK827525AUTOMATIC EXPOSURE CONTROL TYPE A3300K791933CONVERSION CONTRACTOR TIMER KIT

Related Devices (Code: IZL)

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.

K260236XLITEGEMSS HEALTHCARE CO., LTD.K253058Portable DR Imaging SystemShantou Institute of Ultrasonic Instruments Co., Ltd.K260085RAYMO Mobile X-ray System (Model: RAYMO)DRGEM CorporationK253185Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray SystemCarestream HealthK253244AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)Poskom Co., Ltd.K250976Airbile-100Poskom Co., Ltd.

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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