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FDA 510(k)

DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER

K-Number: K901166 · 1990-06-13

ApplicantDalton Technology, Inc.
Decision Date1990-06-13
Product CodeHXX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Dalton Technology, Inc.. It received FDA 510(k) clearance on 1990-06-13 under 510(k) number K901166. The device is classified under product code HXX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER?

DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER is a medical device that received FDA 510(k) clearance on 1990-06-13. The listed applicant is Dalton Technology, Inc.. The 510(k) number is K901166.

When did DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER receive FDA 510(k) clearance?

DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER received FDA 510(k) clearance on 1990-06-13, under 510(k) number K901166.

Who is the listed applicant for DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER?

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

What is the FDA product code for DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER?

The FDA product code for DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER is HXX.

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 Dalton Technology, 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.

K901165MODULAR FLEXIBLE DRILLING SYSTEM

Related Devices (Code: HXX)

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.

K873066ACROMED SCREW DRIVERBuckman Co., Inc.K872389PRECISION SCREW DRIVER SETMed-Tool, Inc.K8626892.5MM HEX DRIVER/CURVE PASSER/BONE PUNCH/RASPW. L. Gore & Associates, 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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