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FDA 510(k)

CAUTERIES, HOT WIRE, DISP.

K-Number: K772199 · 1977-12-13

ApplicantIntermedics, Inc.
Decision Date1977-12-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAUTERIES, HOT WIRE, DISP. is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics, Inc.. It received FDA 510(k) clearance on 1977-12-13 under 510(k) number K772199. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAUTERIES, HOT WIRE, DISP.?

CAUTERIES, HOT WIRE, DISP. is a medical device that received FDA 510(k) clearance on 1977-12-13. The listed applicant is Intermedics, Inc.. The 510(k) number is K772199.

When did CAUTERIES, HOT WIRE, DISP. receive FDA 510(k) clearance?

CAUTERIES, HOT WIRE, DISP. received FDA 510(k) clearance on 1977-12-13, under 510(k) number K772199.

Who is the listed applicant for CAUTERIES, HOT WIRE, DISP.?

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

What is the FDA product code for CAUTERIES, HOT WIRE, DISP.?

The FDA product code for CAUTERIES, HOT WIRE, DISP. is GEI.

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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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