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FDA 510(k)

CHECKPOINT

K-Number: K931947 · 1993-06-18

ApplicantMedical Specialties, Inc.
Decision Date1993-06-18
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CHECKPOINT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialties, Inc.. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K931947. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHECKPOINT?

CHECKPOINT is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K931947.

When did CHECKPOINT receive FDA 510(k) clearance?

CHECKPOINT received FDA 510(k) clearance on 1993-06-18, under 510(k) number K931947.

Who is the listed applicant for CHECKPOINT?

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

What is the FDA product code for CHECKPOINT?

The FDA product code for CHECKPOINT is JPK.

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Other records listing Medical Specialties, 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.

K946201STAND, INFUSIONK926095REFRACTROL-SPK924926MSI-HCTK896566MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVEK883851MSI-CAL 8K883703MSI-CAL 7

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Related Devices (Code: JPK)

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.

K160586XN-L CHECKStreckK160590XN CHECKStreckK160588XN CHECK BFStreckK160606BC-5D Hematology ControlR&D Systems, Inc.K130962R&D 5D RETIC HEMATOLOGY CONTROLR&D Systems, Inc.K120744XN CHECK BFStreck

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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