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FDA 510(k)

ANGIO SYS STERILE FIELD COVER

K-Number: K843257 · 1984-09-21

ApplicantAngiosystems, Inc.
Decision Date1984-09-21
Product Code
DecisionSubstantially Equivalent

Device Summary

ANGIO SYS STERILE FIELD COVER is the device name listed in this FDA 510(k) record. The listed applicant is Angiosystems, Inc.. It received FDA 510(k) clearance on 1984-09-21 under 510(k) number K843257. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIO SYS STERILE FIELD COVER?

ANGIO SYS STERILE FIELD COVER is a medical device that received FDA 510(k) clearance on 1984-09-21. The listed applicant is Angiosystems, Inc.. The 510(k) number is K843257.

When did ANGIO SYS STERILE FIELD COVER receive FDA 510(k) clearance?

ANGIO SYS STERILE FIELD COVER received FDA 510(k) clearance on 1984-09-21, under 510(k) number K843257.

Who is the listed applicant for ANGIO SYS STERILE FIELD COVER?

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

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Other records listing Angiosystems, 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.

K905464MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLINGK905459SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOMK905461PROCEDURE KIT/ROUTINE DENTAL PROCEDURESK905465STERILE DISPOS SURGICAL DRAPE/C-SECTION DRAPEK905466STERILE DISPOSABLE SURGICAL DRAPE/ABDOMINAL DRAPEK905460STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY

View all 14 devices →

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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