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FDA 510(k)

COMPRESSOGRIP ELASTIC STUMP SHRINKER#

K-Number: K831540 · 1983-06-08

ApplicantFred Sammons, Inc.
Decision Date1983-06-08
Product CodeILG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMPRESSOGRIP ELASTIC STUMP SHRINKER# is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831540. The device is classified under product code ILG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSOGRIP ELASTIC STUMP SHRINKER#?

COMPRESSOGRIP ELASTIC STUMP SHRINKER# is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831540.

When did COMPRESSOGRIP ELASTIC STUMP SHRINKER# receive FDA 510(k) clearance?

COMPRESSOGRIP ELASTIC STUMP SHRINKER# received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831540.

Who is the listed applicant for COMPRESSOGRIP ELASTIC STUMP SHRINKER#?

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

What is the FDA product code for COMPRESSOGRIP ELASTIC STUMP SHRINKER#?

The FDA product code for COMPRESSOGRIP ELASTIC STUMP SHRINKER# is ILG.

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Other records listing Fred Sammons, 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.

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGSK831548SPLINTSK831550FINGER BONIOMETER BK7506K831544DELUXE TRACTION EXERCISE GLOVE BK5035

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Related Devices (Code: ILG)

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.

K833437ORTHOPEDIC STOCKINETTENorthern Medical Surgical, Inc.K780612STOCKINETTE, STERILEAbco Dealers, Inc.K780547STERILE ORTHOPEDIC STOCKINETTEAlba-Waldensian, Inc.K770346ORTHOPEDIC STOCKINETTEConvertorsK770173STOCKINETTEChase Mfg. Co.K760817ORTHOPEDIC TUBULAR STOCKINETTEParke-Davis Co.

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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