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FDA 510(k)

SCISSORS GENERAL HOSPITAL

K-Number: K844063 · 1984-11-19

ApplicantI M, Inc.
Decision Date1984-11-19
Product Code
DecisionSubstantially Equivalent

Device Summary

SCISSORS GENERAL HOSPITAL is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K844063. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS GENERAL HOSPITAL?

SCISSORS GENERAL HOSPITAL is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is I M, Inc.. The 510(k) number is K844063.

When did SCISSORS GENERAL HOSPITAL receive FDA 510(k) clearance?

SCISSORS GENERAL HOSPITAL received FDA 510(k) clearance on 1984-11-19, under 510(k) number K844063.

Who is the listed applicant for SCISSORS GENERAL HOSPITAL?

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

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 I M, 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.

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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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