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FDA 510(k)

SAHOTA-KAPLAN HEMOSTAT

K-Number: K823754 · 1983-03-24

ApplicantErickson Industries, Inc.
Decision Date1983-03-24
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SAHOTA-KAPLAN HEMOSTAT is the device name listed in this FDA 510(k) record. The listed applicant is Erickson Industries, Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K823754. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAHOTA-KAPLAN HEMOSTAT?

SAHOTA-KAPLAN HEMOSTAT is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Erickson Industries, Inc.. The 510(k) number is K823754.

When did SAHOTA-KAPLAN HEMOSTAT receive FDA 510(k) clearance?

SAHOTA-KAPLAN HEMOSTAT received FDA 510(k) clearance on 1983-03-24, under 510(k) number K823754.

Who is the listed applicant for SAHOTA-KAPLAN HEMOSTAT?

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

What is the FDA product code for SAHOTA-KAPLAN HEMOSTAT?

The FDA product code for SAHOTA-KAPLAN HEMOSTAT is DQO.

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Related Devices (Code: DQO)

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Official Source

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