MULTI-FLEX TABLE -- MODEL 101
K-Number: K870710 · 1987-06-09
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Device Summary
Frequently Asked Questions
What is the MULTI-FLEX TABLE -- MODEL 101?
MULTI-FLEX TABLE -- MODEL 101 is a medical device that received FDA 510(k) clearance on 1987-06-09. The listed applicant is Slenderizers Equipment Mfg., Inc.. The 510(k) number is K870710.
When did MULTI-FLEX TABLE -- MODEL 101 receive FDA 510(k) clearance?
MULTI-FLEX TABLE -- MODEL 101 received FDA 510(k) clearance on 1987-06-09, under 510(k) number K870710.
Who is the listed applicant for MULTI-FLEX TABLE -- MODEL 101?
The FDA 510(k) record lists Slenderizers Equipment Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI-FLEX TABLE -- MODEL 101?
The FDA product code for MULTI-FLEX TABLE -- MODEL 101 is JFB.
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 Slenderizers Equipment Mfg., 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: JFB)
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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