FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ELMED PNEUMOMAT DIGITAL

K Number: K905417 · Decision Jan 31, 1991
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
26
Review Days
58

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Basic Information

Device Name
ELMED PNEUMOMAT DIGITAL
K Number
K905417
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Elmed, Inc.
Date Received
December 4, 1990
Decision Date
January 31, 1991
Product Code
HIF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIF Insufflator, Laparoscopic

Similar 510(k) Clearances

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

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Other Clearances by Elmed, Inc.

K Number Device Name
K010465 DENSTAT
K974793 ELMED ESU 120 M/M DIGITAL
K953271 ELMED RF-ALERT
K952110 ELMED THERMO-FLUX
K926517 ELMED LBC 50-P
K932938 ELMED ESU 300 M/M AND DIGITAL
K921770 ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M
K915731 ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL
K881431 SIEMENS STEREODYNATOR 828
K875238 SIEMENS NEUROTON 826 AND 827
Search all 26 clearances from Elmed, Inc. →