Cleared Traditional

EXAMINATION & TREATMENT CHAIRS

K822251 · Kelleher Corp. · General & Plastic Surgery

Aug 1982

Decision

29d

Days

Class 1

Risk

About This 510(k) Submission

K822251 is an FDA 510(k) clearance for the EXAMINATION & TREATMENT CHAIRS, a Chair, Surgical, Ac-powered (Class I — General Controls, product code GBB), submitted by Kelleher Corp. (Mchenry, US). The FDA issued a Cleared decision on August 27, 1982, 29 days after receiving the submission on July 29, 1982. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4960.

Submission Details

510(k) Number	K822251 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 29, 1982
Decision Date	August 27, 1982
Days to Decision	29 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—