HAWKEYE OPTION FOR DUAL-HEAD VARIABLE ANGLE GAMMA CAMERA— 510(k) K991841

Substantially Equivalent

Ge Medical Systems F.I. Haifa

FDA 510(k) clearance K991841 for HAWKEYE OPTION FOR DUAL-HEAD VARIABLE ANGLE GAMMA CAMERA, Substantially Equivalent on 1999-08-26. Applicant: Ge Medical Systems F.I. Haifa. Device class: 2.

Clearance details

Applicant
Ge Medical Systems F.I. Haifa
Product code
Code KPS
Device class
Class 2
Regulation
21 CFR 892.1200
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Tirat Hacarmel, IL
Download summary PDFView on FDA.gov ↗

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Recalls naming K991841

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K991841.

Data sourced from openFDA. This site is unofficial and independent of the FDA.