ClearanceBrief
Company ยท US

Gibeck Respiration

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1988. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BYDCondenser, Heat And Moisture (Artificial Nose)6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 24, 1988K881657HUMID-VENT FILTER
Gibeck Respiration
BYD
Jun 16, 1988K881656HUMID-VENT 2 S FLEX
Gibeck Respiration
BYD
Jun 10, 1988K881644HUMID-VENT 2 S
Gibeck Respiration
BYD
Nov 24, 1987K873768HUMID-VENT(R) 2 PORT
Gibeck Respiration
BYD
Nov 6, 1987K873767HUMID-VENT(R) MINI
Gibeck Respiration
BYD
Aug 3, 1987K872153STOM-VENT
Gibeck Respiration
BYD

Latest recalls

DateFirm and productCodeLinked 510(k)
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