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FDA 510(k)

RIA STAT 16

K-Number: K821494 · 1982-06-03

ApplicantE. R. Squibb & Sons, Inc.
Decision Date1982-06-03
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA STAT 16 is the device name listed in this FDA 510(k) record. The listed applicant is E. R. Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1982-06-03 under 510(k) number K821494. 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 RIA STAT 16?

RIA STAT 16 is a medical device that received FDA 510(k) clearance on 1982-06-03. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K821494.

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

RIA STAT 16 received FDA 510(k) clearance on 1982-06-03, under 510(k) number K821494.

Who is the listed applicant for RIA STAT 16?

The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA STAT 16?

The FDA product code for RIA STAT 16 is JJJ.

Other records listing E. R. Squibb & Sons, 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.

K820616ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAYK820340T3 UPTAKE-SQUIBB DIAGNOSTIC KITK820341CORTISOL-SQUIBB RADIOIMMUNOASSAY KITK811240SUR-FIT LOOP OSTOMY O.R. SETK811239SUR-FIT DISPOSABLE CONVEX INSERTK811160SUR-FIT IRRIGATION SLEEVE

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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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