Bunn Model 510 Medication Compressor

by The John Bunn Co. 510(k)

Active United States

510(k) K862628

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK862628	Date7 Aug 1986Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K862628
FDA Product Code: BTI

Device Class: Class II
Regulation: 21 CFR Part 868.6250
Advisory Committee: Anesthesiology
FDA Decision: SESE Substantially Equivalent

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