Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

M6-M

K-Number: K930699 · 1993-08-09

ApplicantX-Cel X-Ray Corp.
Decision Date1993-08-09
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

M6-M is the device name listed in this FDA 510(k) record. The listed applicant is X-Cel X-Ray Corp.. It received FDA 510(k) clearance on 1993-08-09 under 510(k) number K930699. 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 M6-M?

M6-M is a medical device that received FDA 510(k) clearance on 1993-08-09. The listed applicant is X-Cel X-Ray Corp.. The 510(k) number is K930699.

When did M6-M receive FDA 510(k) clearance?

M6-M received FDA 510(k) clearance on 1993-08-09, under 510(k) number K930699.

Who is the listed applicant for M6-M?

The FDA 510(k) record lists X-Cel X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M6-M?

The FDA product code for M6-M is IZL.

Other records listing X-Cel X-Ray 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.

K993958IDX-60 INTRAORAL X-RAYK871116X-CEL X-RAY MODELS ORT90W, ORT90M AND ORT90RK811230X-CELL X-RAY #'S P-75W/P-75M

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.

↑