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FDA 510(k)

CERTAIN MANUAL SURG. INSTRU. ACCESS

K-Number: K833629 · 1984-01-30

ApplicantCimed Intl., Inc.
Decision Date1984-01-30
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CERTAIN MANUAL SURG. INSTRU. ACCESS is the device name listed in this FDA 510(k) record. The listed applicant is Cimed Intl., Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K833629. 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 CERTAIN MANUAL SURG. INSTRU. ACCESS?

CERTAIN MANUAL SURG. INSTRU. ACCESS is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Cimed Intl., Inc.. The 510(k) number is K833629.

When did CERTAIN MANUAL SURG. INSTRU. ACCESS receive FDA 510(k) clearance?

CERTAIN MANUAL SURG. INSTRU. ACCESS received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833629.

Who is the listed applicant for CERTAIN MANUAL SURG. INSTRU. ACCESS?

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

What is the FDA product code for CERTAIN MANUAL SURG. INSTRU. ACCESS?

The FDA product code for CERTAIN MANUAL SURG. INSTRU. ACCESS is HTD.

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Other records listing Cimed 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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