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FDA 510(k)

OMNI

K-Number: K925625 · 1993-08-19

ApplicantBio-Tek Instruments, Inc.
Decision Date1993-08-19
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OMNI is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tek Instruments, Inc.. It received FDA 510(k) clearance on 1993-08-19 under 510(k) number K925625. 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 OMNI?

OMNI is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K925625.

When did OMNI receive FDA 510(k) clearance?

OMNI received FDA 510(k) clearance on 1993-08-19, under 510(k) number K925625.

Who is the listed applicant for OMNI?

The FDA 510(k) record lists Bio-Tek Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMNI?

The FDA product code for OMNI is JJQ.

Other records listing Bio-Tek Instruments, 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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