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FDA 510(k)

THROMBOREL S

K-Number: K872844 · 1987-08-06

ApplicantBehring Diagnostics, Inc.
Decision Date1987-08-06
Product CodeGJS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

THROMBOREL S is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-08-06 under 510(k) number K872844. The device is classified under product code GJS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBOREL S?

THROMBOREL S is a medical device that received FDA 510(k) clearance on 1987-08-06. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K872844.

When did THROMBOREL S receive FDA 510(k) clearance?

THROMBOREL S received FDA 510(k) clearance on 1987-08-06, under 510(k) number K872844.

Who is the listed applicant for THROMBOREL S?

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

What is the FDA product code for THROMBOREL S?

The FDA product code for THROMBOREL S is GJS.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: GJS)

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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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