FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PLEURA BIOPSY DEVICE

K Number: K901995 · Decision Jul 10, 1990
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
47
Applicant Total
46
Review Days
69

Basic Information

Device Name
PLEURA BIOPSY DEVICE
K Number
K901995
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
MILL-ROSE LABORATORY
Date Received
May 2, 1990
Decision Date
July 10, 1990
Product Code
GDM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GDM Needle, Aspiration And Injection, Reusable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GDM), ordered by most recent decision date.

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Other Clearances by MILL-ROSE LABORATORY

K Number Device Name
K983124 MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KIT
K983122 MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) COMBINATION CYTOLOGY/HISTOLOGY PROCEDURAL KIT
K971275 MILL-ROSE DISPOSABLE POLYPECTOMY SNARE
K962736 MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE
K960880 MILL-ROSE BLIND MICROBIOLOGY BRUSH
K954519 WANG TRANSENDOSCOPIC ASPIRATION NEEDLE
K951600 MILL-ROSE ROTATABLE POLYPECTOMY SNARE
K954745 MILL-ROSE RIGID SCOPE CLEANING BRUSHES
K951051 RITE-BITE BIOPSY FORCEPS
K951048 RITE-BITE BIOPSY FORCEPS
Search all 46 clearances from MILL-ROSE LABORATORY →