Stethoscope, Manual
FDA product code LDE · 28 cleared devices
Class 1
Cardiovascular
- Regulation
- 21 CFR 870.1875
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-02-21 – 1994-12-08
LDE
1994-12-08
LDE
1994-11-30
VARIOUS STETHOSCOPES
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LDE
1994-04-26
MANUAL STETOSCOPE
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LDE
1994-03-03
PROSCOPES AND ADSCOPES
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LDE
1992-11-03
STETHOSCOPE COVER
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LDE
1992-10-20
TIMEOSCOPE AND FLEXISCOPE
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LDE
1991-11-07
STETHOSCOPE
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LDE
1991-06-28
MAXI-SCOPE OR ULTRA-SCOPE
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LDE
1991-04-09
VARIOUS TYPES OF STETHOSCOPES
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LDE
1991-03-21
STETHOSCOPE
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LDE
1989-11-15
V*S*R(TM) SCOPE
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LDE
1989-04-21
KAMED STETHOSCOPE
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LDE
1988-07-18
STETH-SHIELD ACCESSORY TO A STETHOSCOPE
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LDE
1987-09-24
VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:
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LDE
1986-08-14
DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE
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LDE
1986-05-09
SALTZMAN STETHOSCOPE HEAD
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LDE
1985-06-06
SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH
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LDE
1985-06-06
LITTMAN TYPE SH-6010, NURSE TYPE
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LDE
1983-07-19
THE BLOOM STETHOSCOPE
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LDE
1982-07-14
LITTMAN TUNABLE STETHOSCOPE 2136
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LDE
1982-01-12
CARDIOSONIC ACOUSTIC AMPLIFIER
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LDE
1981-10-13
AMPLITONE-3
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LDE
1980-09-09
PALPATION ENHANCER
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LDE
1980-06-04
ABCO PEDIATRIC STETHOSCOPE
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LDE
1980-06-04
CONPHAR BOWLS STETHOSCOPE
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LDE
1980-06-04
CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE
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LDE
1980-06-04
CONPHAR DUAL HEAD STETHOSCOPE
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LDE
1978-02-21
BLACK BAG, ELECTRONIC
View details →No matching devices.
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