Atlas FDA

TELESCOPE, RIGID ENDOSCOPE

FDA 510(k) clearance K760177 · decided 1976-08-30

Clearance details

K-number
K760177
Device name
TELESCOPE, RIGID ENDOSCOPE
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Decision
Substantially Equivalent
Date received
1976-07-06
Decision date
1976-08-30
Days to decision
55 days
Clearance type
Traditional
Product code
FBP
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, 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
OES ELITE Telescopes, Protective Tube (K151191)Olympus Winter & Ibe GmbH2015-11-24
ENDOSERVICE ENDOSCOPIC INSTRUMENTS & ACCESSORIES AND MINIMALLY INVASIVE GI AND GU DEVICES (K113062)Endoservice Optical Instruments GmbH2012-08-21
ACMI M4 TELESCOPES (K031758)Acmi Corporation2003-09-02
PANOVIEW PLUS OPTIC WITH 2.7MM DIAMETER, MODEL 8672.XXX, PANOVIEW PLUS OPTIC WITH 1.9MM DIAMETER, MODEL 8686.XXX (K984607)Richard Wolf Medical Instruments Corp.1999-03-05

Recalls involving this device

No recalls on record reference this clearance.