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FDA 510(k)

CAP-RIA 16

K-Number: K823240 · 1982-12-03

ApplicantCapintec, Inc.
Decision Date1982-12-03
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CAP-RIA 16 is the device name listed in this FDA 510(k) record. The listed applicant is Capintec, Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823240. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP-RIA 16?

CAP-RIA 16 is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Capintec, Inc.. The 510(k) number is K823240.

When did CAP-RIA 16 receive FDA 510(k) clearance?

CAP-RIA 16 received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823240.

Who is the listed applicant for CAP-RIA 16?

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

What is the FDA product code for CAP-RIA 16?

The FDA product code for CAP-RIA 16 is JJJ.

Other records listing Capintec, 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.

K192199CRC PC Smart Chamber K1K162394CRC-77tHRK101452CAPINTEC CRC 55T SERIES DOSE CALIBRATORS, MODELS CRC 55TR, CRC 55TPET AND CRC 55TWK071396CRC 25 SERIES (CRC 25R, CRC 25PET, CRC 25W) DOSE CALIBRATORSK052595CRC 15ULTRAK0301752 BASIC

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Related Devices (Code: JJJ)

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.

K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, 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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