21 C.F.R. § 880.6300
Implantable radiofrequency transponder system for patient identification and health information.
Cite as 21 C.F.R. § 880.6300 (2026)
(a)
Identification.
An implantable radiofrequency transponder system for patient identification and health information is a device intended to enable access to secure patient identification and corresponding health information. This system may include a passive implanted transponder, inserter, and scanner. The implanted transponder is used only to store a unique electronic identification code that is read by the scanner. The identification code is used to access patient identity and corresponding health information stored in a database.
(b)
Classification.
Class II (special controls). The special control is FDA's guidance document entitled “Class II Special Controls Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information.” See § 880.1(e) for the availability of this guidance document. This device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 880.9.
[69 FR 71704, Dec. 10, 2004]
- Cross-references to the CFR
- 880.1880.9.