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FDA 510(k)

MOTI PROTECTIVE X-RAY MASK

K-Number: K802377 · 1980-10-31

ApplicantMoti Enterprises, Inc.
Decision Date1980-10-31
Product CodeKPY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOTI PROTECTIVE X-RAY MASK is the device name listed in this FDA 510(k) record. The listed applicant is Moti Enterprises, Inc.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802377. The device is classified under product code KPY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTI PROTECTIVE X-RAY MASK?

MOTI PROTECTIVE X-RAY MASK is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Moti Enterprises, Inc.. The 510(k) number is K802377.

When did MOTI PROTECTIVE X-RAY MASK receive FDA 510(k) clearance?

MOTI PROTECTIVE X-RAY MASK received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802377.

Who is the listed applicant for MOTI PROTECTIVE X-RAY MASK?

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

What is the FDA product code for MOTI PROTECTIVE X-RAY MASK?

The FDA product code for MOTI PROTECTIVE X-RAY MASK is KPY.

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 Moti Enterprises, 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.

K843437MEI MAMMOGRAPHY SYS MX-2049K810095MOTI APRON

Related Devices (Code: KPY)

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.

K110900DISPOSABLE THYROID COLLARBloxr CorporationK962622INTRA-ORAL THERMOPLASTIC SHIELDMedtec, Inc.K954456THERMOPLASTIC SHIELDMedtec, Inc.K954146UTK-DTE AUTILARY SHIELDMallinckrodt MedicalK953610AUKULYTEAukland Medical Plastics, Inc.K9510042001 SPECIAL PROCEDURE LAMP (LOW VOLTAGE) (AS EXHIBITS #2 & 4)Kenex , 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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