• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Compressor, Air, Portable
510(k) Number K850795
Device Name AIR COMPRESSOR
Applicant
BEAR MEDICAL SYSTEMS, INC.
TIMETER INSTRUMENTS CORP.
2501 OREGON PIKE
LANCASTER,  PA  17601
Applicant Contact TERRY L LANDIS
Correspondent
BEAR MEDICAL SYSTEMS, INC.
TIMETER INSTRUMENTS CORP.
2501 OREGON PIKE
LANCASTER,  PA  17601
Correspondent Contact TERRY L LANDIS
Regulation Number868.6250
Classification Product Code
BTI  
Date Received02/07/1985
Decision Date 05/28/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-