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FDA 510(k)

PB-A LEAD-ACID BATTERY CONVERSION KIT

K-Number: K875106 · 1988-02-22

ApplicantDiagnostic Imaging Specialists Corp.
Decision Date1988-02-22
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PB-A LEAD-ACID BATTERY CONVERSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Imaging Specialists Corp.. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K875106. 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 PB-A LEAD-ACID BATTERY CONVERSION KIT?

PB-A LEAD-ACID BATTERY CONVERSION KIT is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Diagnostic Imaging Specialists Corp.. The 510(k) number is K875106.

When did PB-A LEAD-ACID BATTERY CONVERSION KIT receive FDA 510(k) clearance?

PB-A LEAD-ACID BATTERY CONVERSION KIT received FDA 510(k) clearance on 1988-02-22, under 510(k) number K875106.

Who is the listed applicant for PB-A LEAD-ACID BATTERY CONVERSION KIT?

The FDA 510(k) record lists Diagnostic Imaging Specialists Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PB-A LEAD-ACID BATTERY CONVERSION KIT?

The FDA product code for PB-A LEAD-ACID BATTERY CONVERSION KIT 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 Diagnostic Imaging Specialists Corp. 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.

K871592RF-1 CIRCUIT

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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