Needle, Spray

by Richard Wolf Medical Instruments Corp. 510(k)

Active United States

510(k) K770710

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK770710	Date26 Apr 1977Cleared	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Withdrawn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: K770710
FDA Product Code: HRX

Device Class: Class II
Regulation: 21 CFR Part 888.1100
Advisory Committee: Orthopedic
FDA Decision: SESE Substantially Equivalent

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