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FDA 510(k)

IMSI/METRIPOND GRIPPER PLATE

K-Number: K843370 · 1985-01-23

Decision Date1985-01-23
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IMSI/METRIPOND GRIPPER PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Management Services, Inc.. It received FDA 510(k) clearance on 1985-01-23 under 510(k) number K843370. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMSI/METRIPOND GRIPPER PLATE?

IMSI/METRIPOND GRIPPER PLATE is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is Intl. Management Services, Inc.. The 510(k) number is K843370.

When did IMSI/METRIPOND GRIPPER PLATE receive FDA 510(k) clearance?

IMSI/METRIPOND GRIPPER PLATE received FDA 510(k) clearance on 1985-01-23, under 510(k) number K843370.

Who is the listed applicant for IMSI/METRIPOND GRIPPER PLATE?

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

What is the FDA product code for IMSI/METRIPOND GRIPPER PLATE?

The FDA product code for IMSI/METRIPOND GRIPPER PLATE is HRS.

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.

Other records listing Intl. Management Services, 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.

Related Devices (Code: HRS)

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.

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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