RELIANCE MOD-U-LINE M-700
K-Number: K761147 · 1977-01-28
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Device Summary
Frequently Asked Questions
What is the RELIANCE MOD-U-LINE M-700?
RELIANCE MOD-U-LINE M-700 is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is F. & F. Koenigkramer. The 510(k) number is K761147.
When did RELIANCE MOD-U-LINE M-700 receive FDA 510(k) clearance?
RELIANCE MOD-U-LINE M-700 received FDA 510(k) clearance on 1977-01-28, under 510(k) number K761147.
Who is the listed applicant for RELIANCE MOD-U-LINE M-700?
The FDA 510(k) record lists F. & F. Koenigkramer as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RELIANCE MOD-U-LINE M-700?
The FDA product code for RELIANCE MOD-U-LINE M-700 is FPO.
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 F. & F. Koenigkramer 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: FPO)
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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