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FDA 510(k)

DISPOS. ABODOMINAL RETRACTING PAD

K-Number: K831130 · 1983-08-12

ApplicantProduct Development Corp.
Decision Date1983-08-12
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOS. ABODOMINAL RETRACTING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Product Development Corp.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K831130. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS. ABODOMINAL RETRACTING PAD?

DISPOS. ABODOMINAL RETRACTING PAD is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Product Development Corp.. The 510(k) number is K831130.

When did DISPOS. ABODOMINAL RETRACTING PAD receive FDA 510(k) clearance?

DISPOS. ABODOMINAL RETRACTING PAD received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831130.

Who is the listed applicant for DISPOS. ABODOMINAL RETRACTING PAD?

The FDA 510(k) record lists Product Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOS. ABODOMINAL RETRACTING PAD?

The FDA product code for DISPOS. ABODOMINAL RETRACTING PAD is DWF.

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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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