Cleared Traditional

K822251 - EXAMINATION & TREATMENT CHAIRS

K822251 is an FDA 510(k) clearance for EXAMINATION & TREATMENT CHAIRS, manufactured by Kelleher Corp.. The device is a Class 1 General & Plastic Surgery device with product code GBB cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K822251 · Kelleher Corp. · General & Plastic Surgery device
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Aug 1982
Decision
29d
Days
Class 1
Risk

K822251 is an FDA 510(k) clearance for the EXAMINATION & TREATMENT CHAIRS. Classified as Chair, Surgical, Ac-powered (product code GBB), Class I - General Controls.

Submitted by Kelleher Corp. (Mchenry, US). The FDA issued a Cleared decision on August 27, 1982 after a review of 29 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4960 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Kelleher Corp. devices

FDA 510(k) Submission Details - K822251

510(k) Number K822251 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (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 -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
86d faster than avg
Panel avg: 115d · This submission: 29d
Pathway characteristics
Predicate-based equivalence.

GBB Device Classification - Class 1, General Controls

Product Code GBB Chair, Surgical, Ac-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4960
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GBB Chair, Surgical, Ac-powered

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