JARIT SURGICAL INSTRUMENTS— 510(k) K932456
Substantially EquivalentJ. Jamner Surgical Instruments, Inc.
FDA 510(k) clearance K932456 for JARIT SURGICAL INSTRUMENTS, Substantially Equivalent on 1994-04-21. Applicant: J. Jamner Surgical Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- J. Jamner Surgical Instruments, Inc.
- Product code
- Code KNF
- Device class
- Class 2
- Regulation
- 21 CFR 884.4160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
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More clearances from J. Jamner Surgical Instruments, Inc.
view all- K082349 — JARIT HULKA UTERINE TENACULUM FORCEPS
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- K941565 — JARIT RECOMMENDED SINUS INSTRUMENTS
- K933728 — JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-334, 615-335, 615-338, 615-339
Recalls naming K932456
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K932456.
Data sourced from openFDA. This site is unofficial and independent of the FDA.