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FDA 510(k)

GRAB BAR

K-Number: K780935 · 1978-06-19

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1978-06-19
Product CodeIKX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRAB BAR is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-06-19 under 510(k) number K780935. The device is classified under product code IKX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAB BAR?

GRAB BAR is a medical device that received FDA 510(k) clearance on 1978-06-19. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780935.

When did GRAB BAR receive FDA 510(k) clearance?

GRAB BAR received FDA 510(k) clearance on 1978-06-19, under 510(k) number K780935.

Who is the listed applicant for GRAB BAR?

The FDA 510(k) record lists Orthopedic Equipment Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAB BAR?

The FDA product code for GRAB BAR is IKX.

Other records listing Orthopedic Equipment Co., 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.

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COMK841189OEC/REZAIAN SPINAL FIXATORK800530SCHLEIN TRI-SURFACE ANKLEK781445SPREADERK790247TOURNIQUET TEST GAGEK790209FILTER SYSTEM, ALTNER DISPOSABLE

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Related Devices (Code: IKX)

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.

K862895TRICYCLESMednet, Inc.K842650WALL GRAB BARS 98130-98136Guardian Products Co., Inc.K831541TUB TRANSFER BENCH BK6481Fred Sammons, Inc.K823639BOARD TO TRANSFER PARALYZED PATIENT FROMFred Sammons, Inc.K823640BATH TUB SAFETY BARFred Sammons, Inc.K823634CHAIR OR BED LEG EXTENDERSFred Sammons, 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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