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FDA 510(k)

FLEX D-4000

K-Number: K951419 · 1995-06-30

ApplicantU.S. Table, Inc.
Decision Date1995-06-30
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FLEX D-4000 is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Table, Inc.. It received FDA 510(k) clearance on 1995-06-30 under 510(k) number K951419. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX D-4000?

FLEX D-4000 is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is U.S. Table, Inc.. The 510(k) number is K951419.

When did FLEX D-4000 receive FDA 510(k) clearance?

FLEX D-4000 received FDA 510(k) clearance on 1995-06-30, under 510(k) number K951419.

Who is the listed applicant for FLEX D-4000?

The FDA 510(k) record lists U.S. Table, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEX D-4000?

The FDA product code for FLEX D-4000 is INQ.

Other records listing U.S. Table, 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.

K953621EVT-3300K953622PTT 6200 ELEVATION THERAPY TABLEK952600EVT-5000BXK951228ASH-7000

Related Devices (Code: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

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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