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FDA 510(k)

SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE

K-Number: K890503 · 1989-02-10

ApplicantGespac, Inc.
Decision Date1989-02-10
Product CodeGKB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE is the device name listed in this FDA 510(k) record. The listed applicant is Gespac, Inc.. It received FDA 510(k) clearance on 1989-02-10 under 510(k) number K890503. The device is classified under product code GKB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE?

SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE is a medical device that received FDA 510(k) clearance on 1989-02-10. The listed applicant is Gespac, Inc.. The 510(k) number is K890503.

When did SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE receive FDA 510(k) clearance?

SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE received FDA 510(k) clearance on 1989-02-10, under 510(k) number K890503.

Who is the listed applicant for SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE?

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

What is the FDA product code for SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE?

The FDA product code for SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE is GKB.

Related Clinical Trials

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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Other records listing Gespac, 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.

K892522SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED

Related Devices (Code: GKB)

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.

K892522SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIEDGespac, 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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