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FDA 510(k)

AUTOSCAN 3

K-Number: K792647 · 1980-03-17

ApplicantCnr Labs
Decision Date1980-03-17
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOSCAN 3 is the device name listed in this FDA 510(k) record. The listed applicant is Cnr Labs. It received FDA 510(k) clearance on 1980-03-17 under 510(k) number K792647. 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 AUTOSCAN 3?

AUTOSCAN 3 is a medical device that received FDA 510(k) clearance on 1980-03-17. The listed applicant is Cnr Labs. The 510(k) number is K792647.

When did AUTOSCAN 3 receive FDA 510(k) clearance?

AUTOSCAN 3 received FDA 510(k) clearance on 1980-03-17, under 510(k) number K792647.

Who is the listed applicant for AUTOSCAN 3?

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

What is the FDA product code for AUTOSCAN 3?

The FDA product code for AUTOSCAN 3 is JJQ.

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 Cnr Labs 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.

K781368MICRODILUTION GRAM-NEGATIVE ID. PANELK781367MICRODILUTION STREP ID. PANELK781369MICRODILUTION ANAEROBE ID. PANEL

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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