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FDA 510(k)

CURVED HEMOSTAT 5

K-Number: K831138 · 1983-05-18

ApplicantAlmore Intl., Inc.
Decision Date1983-05-18
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CURVED HEMOSTAT 5 is the device name listed in this FDA 510(k) record. The listed applicant is Almore Intl., Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K831138. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURVED HEMOSTAT 5?

CURVED HEMOSTAT 5 is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Almore Intl., Inc.. The 510(k) number is K831138.

When did CURVED HEMOSTAT 5 receive FDA 510(k) clearance?

CURVED HEMOSTAT 5 received FDA 510(k) clearance on 1983-05-18, under 510(k) number K831138.

Who is the listed applicant for CURVED HEMOSTAT 5?

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

What is the FDA product code for CURVED HEMOSTAT 5?

The FDA product code for CURVED HEMOSTAT 5 is HTD.

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Other records listing Almore Intl., 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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Related Devices (Code: HTD)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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