Atlas FDA

DIGITAL MANOMETER (DM 50)

FDA 510(k) clearance K901998 · decided 1990-07-25

Clearance details

K-number
K901998
Device name
DIGITAL MANOMETER (DM 50)
Applicant
Medical Support Products, Inc.
Decision
Substantially Equivalent
Date received
1990-05-02
Decision date
1990-07-25
Days to decision
84 days
Clearance type
Traditional
Product code
BXR
Device class
2
Regulation number
868.1780
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Lancaster, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NS SERIES NIF (NEGATIVE INSPIRATORY FORCE) METERS (K081693)Instrumentation Industries, Inc.2008-09-11
MERCURY MEDICAL NEGATIVE INSPIRATORY FORCE (NIF) DISPOSABLE MONOMETER (K032593)Mercury Medical2004-02-03
COLLINS DIGITAL PULMONARY MANOMETER (K912946)Warren E. Collins, Inc.1992-01-15
THAYER MIP ADAPTER (K904917)Thayer Medical Corp.1991-01-28
INSPIRATORY FORCE MONT KIT/MANIFOLD/METER/TUBING (K873498)Dhd Medical Products Div. Diemolding Corp.1988-03-09

Recalls involving this device

No recalls on record reference this clearance.