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FDA 510(k)

TIP WIPE

K-Number: K811712 · 1981-07-20

Decision Date1981-07-20
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TIP WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811712. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIP WIPE?

TIP WIPE is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Devon Industries, Inc.. The 510(k) number is K811712.

When did TIP WIPE receive FDA 510(k) clearance?

TIP WIPE received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811712.

Who is the listed applicant for TIP WIPE?

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

What is the FDA product code for TIP WIPE?

The FDA product code for TIP WIPE is KDC.

Other records listing Devon Industries, 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.

View all 47 devices →

Related Devices (Code: KDC)

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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