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

SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM

K Number: K896630 · Decision Jun 6, 1990
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
18
Applicant Total
15
Review Days
196

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM
K Number
K896630
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Atos Medical AB
Date Received
November 22, 1989
Decision Date
June 6, 1990
Product Code
KAM
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
KAM Cannula, Sinus

Similar 510(k) Clearances

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

View all

Other Clearances by Atos Medical AB

K Number Device Name
K151404 ProTrach Dualcare
K141380 PROVOX FREEHANDS FLEXIVOICE
K131947 PROVOX VEGA PUNCTURE SET
K092593 PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM)
K090455 PROVOX VEGA, MODEL 8130-8135
K072582 PROVOX MICRON HME
K043138 PROVOX NID VOICE REHABILITATION SYSTEM, MODEL REF 7101 TO 7134
K022125 PROVOX FREEHANDS HME, MODEL 7710
K014102 PROVOX HME CASSETTE, MODEL 7240; PROVOX ADHESIVE, MODEL 7251
K971244 PROVOX 2 VOICE PROSTHESIS SYSTEM
Search all 15 clearances from Atos Medical AB →