GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25 (K012869) — FDA 510(k) Clearance | Predicase

K-number	K012869
Device name	GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25
Applicant	Gimmi GmbH
Product code	HIH
Device class	Class II
Decision date	Mar 11, 2002
Decision	Substantially Equivalent
Regulation	884.1690

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