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FDA 510(k)

TILT 10, CATALOG #S-2600

K-Number: K771942 · 1977-10-27

ApplicantAffiliated Hospital Products, Inc.
Decision Date1977-10-27
Product CodeHDD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TILT 10, CATALOG #S-2600 is the device name listed in this FDA 510(k) record. The listed applicant is Affiliated Hospital Products, Inc.. It received FDA 510(k) clearance on 1977-10-27 under 510(k) number K771942. The device is classified under product code HDD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TILT 10, CATALOG #S-2600?

TILT 10, CATALOG #S-2600 is a medical device that received FDA 510(k) clearance on 1977-10-27. The listed applicant is Affiliated Hospital Products, Inc.. The 510(k) number is K771942.

When did TILT 10, CATALOG #S-2600 receive FDA 510(k) clearance?

TILT 10, CATALOG #S-2600 received FDA 510(k) clearance on 1977-10-27, under 510(k) number K771942.

Who is the listed applicant for TILT 10, CATALOG #S-2600?

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

What is the FDA product code for TILT 10, CATALOG #S-2600?

The FDA product code for TILT 10, CATALOG #S-2600 is HDD.

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Other records listing Affiliated Hospital Products, 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.

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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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