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FDA 510(k)

PROXIMATE (TMD) TISSUE MEASURING DEVICE

K-Number: K801374 · 1980-06-26

ApplicantETHICON, Inc.
Decision Date1980-06-26
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROXIMATE (TMD) TISSUE MEASURING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1980-06-26 under 510(k) number K801374. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROXIMATE (TMD) TISSUE MEASURING DEVICE?

PROXIMATE (TMD) TISSUE MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1980-06-26. The listed applicant is ETHICON, Inc.. The 510(k) number is K801374.

When did PROXIMATE (TMD) TISSUE MEASURING DEVICE receive FDA 510(k) clearance?

PROXIMATE (TMD) TISSUE MEASURING DEVICE received FDA 510(k) clearance on 1980-06-26, under 510(k) number K801374.

Who is the listed applicant for PROXIMATE (TMD) TISSUE MEASURING DEVICE?

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

What is the FDA product code for PROXIMATE (TMD) TISSUE MEASURING DEVICE?

The FDA product code for PROXIMATE (TMD) TISSUE MEASURING DEVICE is FTY.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: FTY)

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.

K160501Noxilizer Surgical RulerNoxilizer, Inc.K951064DISPOSABLE WOUND MEASURE GUIDE, PLASTIC, PROTECTOR, WOUND, PLASTICS-E Sales & Distribution, Inc.K934930OLYMPIC AUTO-LENGTHOlympic Medical Corp.K932112OLYMPIC INFA-LENGTHOlympic Medical Corp.K883485STRYKER PRESSURE MONITOR SYSTEMStryker Corp.K880441PEDIATRIC AIRWAY MEASUREMENT SYSTEM & P.A.M.S.Plane Iii, 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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