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FDA 510(k)

MOTORIZED DEPTH DOSE APPARATUS

K-Number: K943199 · 1994-12-07

ApplicantMedtec, Inc.
Decision Date1994-12-07
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOTORIZED DEPTH DOSE APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K943199. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTORIZED DEPTH DOSE APPARATUS?

MOTORIZED DEPTH DOSE APPARATUS is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Medtec, Inc.. The 510(k) number is K943199.

When did MOTORIZED DEPTH DOSE APPARATUS receive FDA 510(k) clearance?

MOTORIZED DEPTH DOSE APPARATUS received FDA 510(k) clearance on 1994-12-07, under 510(k) number K943199.

Who is the listed applicant for MOTORIZED DEPTH DOSE APPARATUS?

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

What is the FDA product code for MOTORIZED DEPTH DOSE APPARATUS?

The FDA product code for MOTORIZED DEPTH DOSE APPARATUS is IYE.

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Other records listing Medtec, 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.

K111340HEAD AND NECK IMMOBILIZATION SYSTEM, BODY IMMOBILIZATION SYSTEMK093738MRI PATIENT POSITIONING DEVICESK974703CARBON FIBER BREAST BOARDK974700MATRIX MT-MX3K973842CARBON FIBER CONFORMAL COUCH TOPK962622INTRA-ORAL THERMOPLASTIC SHIELD

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Related Devices (Code: IYE)

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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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