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FDA 510(k)

SHUR-GRIP

K-Number: K912834 · 1991-07-26

ApplicantInman Medical Corp.
Decision Date1991-07-26
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHUR-GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K912834. 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 SHUR-GRIP?

SHUR-GRIP is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Inman Medical Corp.. The 510(k) number is K912834.

When did SHUR-GRIP receive FDA 510(k) clearance?

SHUR-GRIP received FDA 510(k) clearance on 1991-07-26, under 510(k) number K912834.

Who is the listed applicant for SHUR-GRIP?

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

What is the FDA product code for SHUR-GRIP?

The FDA product code for SHUR-GRIP is KDC.

Other records listing Inman Medical Corp. 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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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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