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FDA 510(k)

RELIANCE MOD-U-LINE M-700

K-Number: K761147 · 1977-01-28

Decision Date1977-01-28
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RELIANCE MOD-U-LINE M-700 is the device name listed in this FDA 510(k) record. The listed applicant is F. & F. Koenigkramer. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K761147. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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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