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FDA 510(k)

REX-CAPS

K-Number: K823098 · 1982-11-10

ApplicantBauer, Cheng & Associates, Inc.
Decision Date1982-11-10
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REX-CAPS is the device name listed in this FDA 510(k) record. The listed applicant is Bauer, Cheng & Associates, Inc.. It received FDA 510(k) clearance on 1982-11-10 under 510(k) number K823098. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REX-CAPS?

REX-CAPS is a medical device that received FDA 510(k) clearance on 1982-11-10. The listed applicant is Bauer, Cheng & Associates, Inc.. The 510(k) number is K823098.

When did REX-CAPS receive FDA 510(k) clearance?

REX-CAPS received FDA 510(k) clearance on 1982-11-10, under 510(k) number K823098.

Who is the listed applicant for REX-CAPS?

The FDA 510(k) record lists Bauer, Cheng & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REX-CAPS?

The FDA product code for REX-CAPS is EJJ.

Other records listing Bauer, Cheng & Associates, 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.

K840084COLTENE BRILLIANT LUXK840085COLTENE BRILLIANTK823100RX 91K823097NATURELLEK823084CHALLENGERK823099RX MIDACAST

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Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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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