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FDA 510(k)

TABLE, SAMPLE IL 461

K-Number: K760233 · 1976-08-26

ApplicantInstrumentation Laboratory CO
Decision Date1976-08-26
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TABLE, SAMPLE IL 461 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760233. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, SAMPLE IL 461?

TABLE, SAMPLE IL 461 is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760233.

When did TABLE, SAMPLE IL 461 receive FDA 510(k) clearance?

TABLE, SAMPLE IL 461 received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760233.

Who is the listed applicant for TABLE, SAMPLE IL 461?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TABLE, SAMPLE IL 461?

The FDA product code for TABLE, SAMPLE IL 461 is JJQ.

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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 Instrumentation Laboratory CO 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.

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Related Devices (Code: JJQ)

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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