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FDA 510(k)

ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.

K-Number: K932857 · 1993-09-13

ApplicantAnsley Medical Products, Inc.
Decision Date1993-09-13
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC. is the device name listed in this FDA 510(k) record. The listed applicant is Ansley Medical Products, Inc.. It received FDA 510(k) clearance on 1993-09-13 under 510(k) number K932857. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.?

ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC. is a medical device that received FDA 510(k) clearance on 1993-09-13. The listed applicant is Ansley Medical Products, Inc.. The 510(k) number is K932857.

When did ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC. receive FDA 510(k) clearance?

ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC. received FDA 510(k) clearance on 1993-09-13, under 510(k) number K932857.

Who is the listed applicant for ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.?

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

What is the FDA product code for ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.?

The FDA product code for ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC. is KKX.

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Other records listing Ansley Medical Products, 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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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