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FDA 510(k)

VESSEL LOOPS

K-Number: K895682 · 1989-10-24

ApplicantApplied Medical Technologies
Decision Date1989-10-24
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VESSEL LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1989-10-24 under 510(k) number K895682. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESSEL LOOPS?

VESSEL LOOPS is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Applied Medical Technologies. The 510(k) number is K895682.

When did VESSEL LOOPS receive FDA 510(k) clearance?

VESSEL LOOPS received FDA 510(k) clearance on 1989-10-24, under 510(k) number K895682.

Who is the listed applicant for VESSEL LOOPS?

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

What is the FDA product code for VESSEL LOOPS?

The FDA product code for VESSEL LOOPS is GDX.

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Other records listing Applied Medical Technologies as applicant

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Related Devices (Code: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K921167ULTRABLADEMicron Technology, Inc.K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K893033MINI-DIAMOND KNIFEL.A.B. Instruments

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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