FDA 510(k)

BALL TIP, MODEL #030-185

K-Number: K770284 · 1977-02-24

Decision Date1977-02-24

Product CodeDTB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BALL TIP, MODEL #030-185 is the device name listed in this FDA 510(k) record. The listed applicant is Med Telectronics , Ltd.. It received FDA 510(k) clearance on 1977-02-24 under 510(k) number K770284. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BALL TIP, MODEL #030-185?

BALL TIP, MODEL #030-185 is a medical device that received FDA 510(k) clearance on 1977-02-24. The listed applicant is Med Telectronics , Ltd.. The 510(k) number is K770284.

When did BALL TIP, MODEL #030-185 receive FDA 510(k) clearance?

BALL TIP, MODEL #030-185 received FDA 510(k) clearance on 1977-02-24, under 510(k) number K770284.

Who is the listed applicant for BALL TIP, MODEL #030-185?

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

What is the FDA product code for BALL TIP, MODEL #030-185?

The FDA product code for BALL TIP, MODEL #030-185 is DTB.

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Other records listing Med Telectronics , Ltd. as applicant

K770661GENERATOR, PULSE, IMPLANTABLE K770282WEDGE TIP, SMALL, MODEL #030-191 K770285BALL TIP, MODEL #030-188 K770283WEDGE TIP, SMALL, MODEL #030-194

Related Devices (Code: DTB)

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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.