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FDA 510(k)

CAUTERY CADDY PAD

K-Number: K811824 · 1981-07-20

ApplicantInstranetics, Inc.
Decision Date1981-07-20
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAUTERY CADDY PAD is the device name listed in this FDA 510(k) record. The listed applicant is Instranetics, Inc.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811824. 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 CAUTERY CADDY PAD?

CAUTERY CADDY PAD is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Instranetics, Inc.. The 510(k) number is K811824.

When did CAUTERY CADDY PAD receive FDA 510(k) clearance?

CAUTERY CADDY PAD received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811824.

Who is the listed applicant for CAUTERY CADDY PAD?

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

What is the FDA product code for CAUTERY CADDY PAD?

The FDA product code for CAUTERY CADDY PAD is KDC.

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.

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Other records listing Instranetics, 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.

K823430INSTRA-SAFEK811822TIP-VUK811823SHARPS CADDY FBK810294LINE CADDYK810208BLADE SAFEK802865SAFE T COUNT

View all 10 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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.

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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