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FDA 510(k)

IMSI/METRIPOND HAND OPERATING TABLE

K-Number: K830339 · 1983-04-12

Decision Date1983-04-12
Product CodeFSE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMSI/METRIPOND HAND OPERATING TABLE 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 1983-04-12 under 510(k) number K830339. The device is classified under product code FSE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMSI/METRIPOND HAND OPERATING TABLE?

IMSI/METRIPOND HAND OPERATING TABLE is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Intl. Management Services, Inc.. The 510(k) number is K830339.

When did IMSI/METRIPOND HAND OPERATING TABLE receive FDA 510(k) clearance?

IMSI/METRIPOND HAND OPERATING TABLE received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830339.

Who is the listed applicant for IMSI/METRIPOND HAND OPERATING TABLE?

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 HAND OPERATING TABLE?

The FDA product code for IMSI/METRIPOND HAND OPERATING TABLE is FSE.

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: FSE)

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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