DIGICAM LHP (VIDEO INTERFACE OPTION)
K-Number: K895668 · 1989-11-15
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Device Summary
Frequently Asked Questions
What is the DIGICAM LHP (VIDEO INTERFACE OPTION)?
DIGICAM LHP (VIDEO INTERFACE OPTION) is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K895668.
When did DIGICAM LHP (VIDEO INTERFACE OPTION) receive FDA 510(k) clearance?
DIGICAM LHP (VIDEO INTERFACE OPTION) received FDA 510(k) clearance on 1989-11-15, under 510(k) number K895668.
Who is the listed applicant for DIGICAM LHP (VIDEO INTERFACE OPTION)?
The FDA 510(k) record lists Siemens Gammasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGICAM LHP (VIDEO INTERFACE OPTION)?
The FDA product code for DIGICAM LHP (VIDEO INTERFACE OPTION) is LMC.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Siemens Gammasonics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LMC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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