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FDA 510(k)

CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD

K-Number: K893454 · 1989-07-25

Decision Date1989-07-25
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD is the device name listed in this FDA 510(k) record. The listed applicant is Atlantic Industries, Inc.. It received FDA 510(k) clearance on 1989-07-25 under 510(k) number K893454. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD?

CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Atlantic Industries, Inc.. The 510(k) number is K893454.

When did CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD receive FDA 510(k) clearance?

CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD received FDA 510(k) clearance on 1989-07-25, under 510(k) number K893454.

Who is the listed applicant for CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD?

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

What is the FDA product code for CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD?

The FDA product code for CHAIR/STOOL UNIT DENTAL OPER., PORTABLE, FIELD is KLC.

Related Clinical Trials

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.

Related Devices (Code: KLC)

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.

Official Source

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