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FDA 510(k)

PERI-K PAD COLD PACK

K-Number: K920760 · 1993-07-29

ApplicantBaxter Healthcare Corp
Decision Date1993-07-29
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERI-K PAD COLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1993-07-29 under 510(k) number K920760. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERI-K PAD COLD PACK?

PERI-K PAD COLD PACK is a medical device that received FDA 510(k) clearance on 1993-07-29. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K920760.

When did PERI-K PAD COLD PACK receive FDA 510(k) clearance?

PERI-K PAD COLD PACK received FDA 510(k) clearance on 1993-07-29, under 510(k) number K920760.

Who is the listed applicant for PERI-K PAD COLD PACK?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERI-K PAD COLD PACK?

The FDA product code for PERI-K PAD COLD PACK is IMD.

Other records listing Baxter Healthcare Corp 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.

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Related Devices (Code: IMD)

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.

K221653InfaTherm Disposable Infant Warming MattressInternational BiomedicalK163295Infant Transport Mattress Warmer with DiscRapid Aid Corp.K112547NEO NESTDenovo Proucts, LLCK082087EYEFEEL OPHTHALMIC WARMERBio-Lipid, Inc.K071710BENGAY (R) HEAT THERAPY, PAIN RELIEVING PATCHES/PADS (VARIOUS)Johnson & Johnson Consumer Products, Inc.K021843EYEFEEL OPHTHALMIC WARMERBio-Lipid, 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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