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FDA 510(k)

AUTO-CLIP

K-Number: K771021 · 1977-06-14

ApplicantAxiom Medical, Inc.
Decision Date1977-06-14
Product CodeDSS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTO-CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Axiom Medical, Inc.. It received FDA 510(k) clearance on 1977-06-14 under 510(k) number K771021. The device is classified under product code DSS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-CLIP?

AUTO-CLIP is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Axiom Medical, Inc.. The 510(k) number is K771021.

When did AUTO-CLIP receive FDA 510(k) clearance?

AUTO-CLIP received FDA 510(k) clearance on 1977-06-14, under 510(k) number K771021.

Who is the listed applicant for AUTO-CLIP?

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

What is the FDA product code for AUTO-CLIP?

The FDA product code for AUTO-CLIP is DSS.

Other records listing Axiom Medical, 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.

K993592AXIOM MULTIPURPOSE WOUND DRAINK971851INTERPLEURAL ANESTHESIA CATHETERK965146FLAT CLOSED WOUND DRAIN WITH TROCARK934895GLASSMAN SILICONE CATHETERK922760ATRAUM WOUND DRESSING--MODIFICATIONK905422PVC ROUND WOUND DRAINS

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Related Devices (Code: DSS)

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.

K983744MCAS (MODULAR CLIP APPLIER SYSTEM)Applied Medical ResourcesK961333HEARTPORT MULTIFIRE CLIP APPLIERHeartport, Inc.K920104IDENTI LOOPS DEGANIA SILICONEPuritas Health Care, Inc.K920676RMI SOFCLAMPResearch Medical, Inc.K914523CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COILCatheter Research C/O Burditt, Bowles & RadziusK901303HORIZON SURGICAL LIGATING AND MARKING CLIPHorizon Surgical, 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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