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FDA 510(k)

STRAIGHT 5 HEMOSTAT

K-Number: K831137 · 1983-05-18

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

Device Summary

STRAIGHT 5 HEMOSTAT 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 K831137. 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 STRAIGHT 5 HEMOSTAT?

STRAIGHT 5 HEMOSTAT 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 K831137.

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

STRAIGHT 5 HEMOSTAT received FDA 510(k) clearance on 1983-05-18, under 510(k) number K831137.

Who is the listed applicant for STRAIGHT 5 HEMOSTAT?

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 STRAIGHT 5 HEMOSTAT?

The FDA product code for STRAIGHT 5 HEMOSTAT 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)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.

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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