ABDOMINAL OR C-SECTION DRAPE SHEET
K-Number: K902384 · 1990-08-09
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Device Summary
Frequently Asked Questions
What is the ABDOMINAL OR C-SECTION DRAPE SHEET?
ABDOMINAL OR C-SECTION DRAPE SHEET is a medical device that received FDA 510(k) clearance on 1990-08-09. The listed applicant is Medical Plastics, Inc.. The 510(k) number is K902384.
When did ABDOMINAL OR C-SECTION DRAPE SHEET receive FDA 510(k) clearance?
ABDOMINAL OR C-SECTION DRAPE SHEET received FDA 510(k) clearance on 1990-08-09, under 510(k) number K902384.
Who is the listed applicant for ABDOMINAL OR C-SECTION DRAPE SHEET?
The FDA 510(k) record lists Medical Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABDOMINAL OR C-SECTION DRAPE SHEET?
The FDA product code for ABDOMINAL OR C-SECTION DRAPE SHEET is KKX.
Related Clinical Trials
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.
Other records listing Medical Plastics, 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.
Related Devices (Code: KKX)
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.
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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