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FDA 510(k)

TYTIN

K-Number: K935535 · 1994-03-11

ApplicantKerr Corporation (Danbury)
Decision Date1994-03-11
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TYTIN is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation (Danbury). It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K935535. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYTIN?

TYTIN is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K935535.

When did TYTIN receive FDA 510(k) clearance?

TYTIN received FDA 510(k) clearance on 1994-03-11, under 510(k) number K935535.

Who is the listed applicant for TYTIN?

The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYTIN?

The FDA product code for TYTIN is EJJ.

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Other records listing Kerr Corporation (Danbury) 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.

K051545L.E. DEMETRON IIK020091OPTILUX 501K951663TYTIN RK951511TYTIN ADMIXK942480M4 CONTRA-ANGLE HANDPIECEK940513OPTIBOND

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Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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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