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FDA 510(k)

CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE

K-Number: K854724 · 1985-12-13

ApplicantLifetrac, Inc.
Decision Date1985-12-13
Product CodeKIZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Lifetrac, Inc.. It received FDA 510(k) clearance on 1985-12-13 under 510(k) number K854724. The device is classified under product code KIZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE?

CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE is a medical device that received FDA 510(k) clearance on 1985-12-13. The listed applicant is Lifetrac, Inc.. The 510(k) number is K854724.

When did CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE receive FDA 510(k) clearance?

CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE received FDA 510(k) clearance on 1985-12-13, under 510(k) number K854724.

Who is the listed applicant for CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE?

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

What is the FDA product code for CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE?

The FDA product code for CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE is KIZ.

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Related Devices (Code: KIZ)

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.

K890542MULTIWELL CULTURE PLATE INSERTSBd Becton Dickinson Vacutainer Systems PreanalyticK873891TISSUE CULTURE DISHESNunc, Inc.K871483TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHESIsratech Marketing Corp.K853634CORNING CELL WELLS-MULTIPLE WELL PLATESCorning Medical & ScientificK821687REMOVAWELL TISSUE CULTURE PLATE W/LIDDynatech Corp.K790958120 WELL HISTO-PLATEDynatech Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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