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FDA 510(k)

ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER

K-Number: K843460 · 1984-09-26

ApplicantVarian Assoc., Inc.
Decision Date1984-09-26
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1984-09-26 under 510(k) number K843460. 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 ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER?

ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1984-09-26. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K843460.

When did ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER receive FDA 510(k) clearance?

ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER received FDA 510(k) clearance on 1984-09-26, under 510(k) number K843460.

Who is the listed applicant for ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER?

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

What is the FDA product code for ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER?

The FDA product code for ULTRAVIOLET-VISIBLE SPECTROPHOTOMETER is JJQ.

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Other records listing Varian Assoc., Inc. as applicant

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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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