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FDA 510(k)

LEAD APRON

K-Number: K931269 · 1993-06-02

ApplicantBt Medical Co., Inc.
Decision Date1993-06-02
Product CodeEAJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LEAD APRON is the device name listed in this FDA 510(k) record. The listed applicant is Bt Medical Co., Inc.. It received FDA 510(k) clearance on 1993-06-02 under 510(k) number K931269. The device is classified under product code EAJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEAD APRON?

LEAD APRON is a medical device that received FDA 510(k) clearance on 1993-06-02. The listed applicant is Bt Medical Co., Inc.. The 510(k) number is K931269.

When did LEAD APRON receive FDA 510(k) clearance?

LEAD APRON received FDA 510(k) clearance on 1993-06-02, under 510(k) number K931269.

Who is the listed applicant for LEAD APRON?

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

What is the FDA product code for LEAD APRON?

The FDA product code for LEAD APRON is EAJ.

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 Bt Medical Co., 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.

K931268URETERAL COMPRESSION DEVICEK930885PNEUMATIC COMPRESSION DEVICEK915321BTM-200 (PROPOSED) POWERED MUSCLE STIMULATORK914999BTM-100 POWERED MUSCLE STIMULATOR (PROPOSED)

Related Devices (Code: EAJ)

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.

K913621RINN PROTECTIVE X-RAY APRON AND PROTECTIVE COLLARRinn Dental ProductsK870563X-RAY APRONX-Tech, Ltd.K870103LEAD APRON CADDYOrthopedic Systems, Inc.K832602THYROID PROTECTIVE COLLARE.M. AdamsK832601LEADED X-RAY APRONE.M. Adams

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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