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FDA 510(k)

PERI-COMFORT(TM) SEATING CUSHION

K-Number: K932396 · 1993-09-30

ApplicantChi'Am Intl.
Decision Date1993-09-30
Product CodeLRL
DecisionSubstantially Equivalent

Device Summary

PERI-COMFORT(TM) SEATING CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Chi'Am Intl.. It received FDA 510(k) clearance on 1993-09-30 under 510(k) number K932396. The device is classified under product code LRL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERI-COMFORT(TM) SEATING CUSHION?

PERI-COMFORT(TM) SEATING CUSHION is a medical device that received FDA 510(k) clearance on 1993-09-30. The listed applicant is Chi'Am Intl.. The 510(k) number is K932396.

When did PERI-COMFORT(TM) SEATING CUSHION receive FDA 510(k) clearance?

PERI-COMFORT(TM) SEATING CUSHION received FDA 510(k) clearance on 1993-09-30, under 510(k) number K932396.

Who is the listed applicant for PERI-COMFORT(TM) SEATING CUSHION?

The FDA 510(k) record lists Chi'Am Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERI-COMFORT(TM) SEATING CUSHION?

The FDA product code for PERI-COMFORT(TM) SEATING CUSHION is LRL.

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Related Devices (Code: LRL)

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.

K072690HEMAWAY SEATHemaway, LLCK864470HEMOREST(TM)Health Aid Products

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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