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FDA 510(k)

SYNELISA RO ABS / LA ABS

K-Number: K930209 · 1993-06-11

ApplicantElias U.S.A., Inc.
Decision Date1993-06-11
Product CodeLJM
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

SYNELISA RO ABS / LA ABS is the device name listed in this FDA 510(k) record. The listed applicant is Elias U.S.A., Inc.. It received FDA 510(k) clearance on 1993-06-11 under 510(k) number K930209. The device is classified under product code LJM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNELISA RO ABS / LA ABS?

SYNELISA RO ABS / LA ABS is a medical device that received FDA 510(k) clearance on 1993-06-11. The listed applicant is Elias U.S.A., Inc.. The 510(k) number is K930209.

When did SYNELISA RO ABS / LA ABS receive FDA 510(k) clearance?

SYNELISA RO ABS / LA ABS received FDA 510(k) clearance on 1993-06-11, under 510(k) number K930209.

Who is the listed applicant for SYNELISA RO ABS / LA ABS?

The FDA 510(k) record lists Elias U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNELISA RO ABS / LA ABS?

The FDA product code for SYNELISA RO ABS / LA ABS is LJM.

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Other records listing Elias U.S.A., Inc. as applicant

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K964385ELIAS ANA-HEP-2K963291VARELISA ANA (4) PROFILEK953873VARELISA HELICOBACTER PYLORI ANTIBODIESK953587VARELISA MPO-ANCAK953586VARELISA PR3-ANCAK951187VARELISA CARDIOLIPIN ABS SCREEN

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Related Devices (Code: LJM)

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.

K182353EliA CENP Immunoassay, EliA U1RNP Immunoassay, EliA RNP70 ImmunoassayPhadia ABK151559ImmuLisa Enhanced Centromere Antibody ELISAImmco Diagnostics, Inc.K131185ANA SCREEN ELISA (IGG)Euroimmun USK083188VARELISA RECOMBI ANA SCREEN, MODEL 12 596Phadia US, Inc.K050967VARELISA RECOMBI CTD SCREEN, MODEL 13096Sweden Diagnostics (Germany) GmbHK050625VARELISA RECOMBI ANA PROFILE, MODEL 18496Sweden Diagnostics (Germany) GmbH

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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