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FDA 510(k)

SLT SPECTRA

K-Number: K915689 · 1992-04-22

ApplicantSlt Labinstruments, Inc.
Decision Date1992-04-22
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SLT SPECTRA is the device name listed in this FDA 510(k) record. The listed applicant is Slt Labinstruments, Inc.. It received FDA 510(k) clearance on 1992-04-22 under 510(k) number K915689. 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 SLT SPECTRA?

SLT SPECTRA is a medical device that received FDA 510(k) clearance on 1992-04-22. The listed applicant is Slt Labinstruments, Inc.. The 510(k) number is K915689.

When did SLT SPECTRA receive FDA 510(k) clearance?

SLT SPECTRA received FDA 510(k) clearance on 1992-04-22, under 510(k) number K915689.

Who is the listed applicant for SLT SPECTRA?

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

What is the FDA product code for SLT SPECTRA?

The FDA product code for SLT SPECTRA is JJQ.

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Other records listing Slt Labinstruments, 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.

K915690SLT 340 ATTCK902776SPECTROPHOTOMETER (MICROASSAY PLATE READERS)K881797EASY WASHER II MICROPLATE WASHERK873678SPECTROPHOTOMETER (MICROASSAY PLATE READERS)K844894PHOTOMETER VARIOUS ONE FOR MICROTITERPLATESK844892SLT 220 WASHER FOR MICROITITERPLATES

View all 9 devices →

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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