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FDA 510(k)

THROMBO PLUS

K-Number: K834527 · 1984-01-30

ApplicantW. Sarstedt, Inc.
Decision Date1984-01-30
Product CodeGGK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

THROMBO PLUS is the device name listed in this FDA 510(k) record. The listed applicant is W. Sarstedt, Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834527. The device is classified under product code GGK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBO PLUS?

THROMBO PLUS is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is W. Sarstedt, Inc.. The 510(k) number is K834527.

When did THROMBO PLUS receive FDA 510(k) clearance?

THROMBO PLUS received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834527.

Who is the listed applicant for THROMBO PLUS?

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

What is the FDA product code for THROMBO PLUS?

The FDA product code for THROMBO PLUS is GGK.

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Related Devices (Code: GGK)

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.

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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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